Life Sciences Regulation News

FDA Latest News
	What's New in Food
	Food safety and nutrition announcements, and newly posted documents on the FDA/Foods website.
FDA CDRH Latest News
	Federal Register: Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications.
	The FDA is is publishing a list of premarket approval applications (PMAs) that have been approved. This list is intended to inform the public of the availability of safety and effectiveness summaries of approved PMAs through the Internet and the...
	Guidance for Industry and FDA Staff - Impact-Resistant Lenses: Questions and Answers
	Eyeglasses and sunglasses (eyewear) that are intended to affect the structure or function of the body or intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, are devices...
	Federal Register: Guidance for Industry and Food and Drug Administration Staff; Impact-Resistant Lenses: Questions and Answers; Availability.
	The FDA is announcing the availability of the guidance entitled 'Impact-Resistant Lenses: Questions and Answers.' This guidance document answers manufacturer, importer, and consumer questions on impact-resistant lenses, including questions on test...
	Office of Device Evaluation Annual Performance Report Fiscal Year 2009
	In the past, the ODE Annual Report included information from and about the ODE Review Divisions, our initiatives, and data analysis from the ODE Program Operations Staff (POS). The FY 09 Report only includes data from POS on our premarket review program.
	Federal Register: Medical Device User Fee Act; Public Meeting; Request for Comments; Amendment of Notice
	The FDA is announcing an amendment to the notice of a public meeting on the reauthorization of the medical device user fee program. This meeting was announced in the Federal Register of August 13, 2010 (75 FR 49502). The amendment is being made to...
	Federal Register: Public Workshop on Medical Devices and Nanotechnology: Manufacturing, Characterization, and Biocompatibility Considerations; Correction.
	The FDA is correcting a notice that appeared in the Federal Register of August 23, 2010 (75 FR 51829). The notice announced the public workshop entitled 'Medical Devices & Nanotechnology: Manufacturing, Characterization, and Biocompatibility...
	FDA Safety Notification: Mammography Problems at Medisound, Inc. in Kissimmee, Florida
	The FDA has become aware of problems associated with the quality of mammograms performed at the Medisound, Inc. facility, located at 301 North John Young Parkway, Kissimmee, Florida 34741...
	CDRH Preliminary Internal Evaluations on the 510(k) Program and the Use of Science in Regulatory Decision Making (Webinar Information Updated)
	FDA has published a notice in the Federal Register requesting public comment on these reports. Please see Docket No. FDA-2010-N-0348, "Center for Devices and Radiological Health 510(k) Working Group Preliminary Report and Recommendations, and Task Force..
	Class I Medical Device Recall: Multi-Med, Inc., 22 Gauge x 1 inch Straight and Right Angle Huber Needles and Navilyst Medical Inc., Vaxcel Implantable Vascular Access Systems Containing Huber Needles (Two Class I Recalls)
	Huber needles are safety needles used on vascular access ports implanted in patients in need of repeated intravenous therapy. A "coring" Huber needle could damage the implanted port by removing silicone slivers from the access membrane...
	Safety Investigation of Non-Coring (Huber) Needles: Updated August 26, 2010
	Huber needles are used to access ports implanted under the skin of chronically ill patients for repeated access to veins for the withdrawal of blood and infusion of medication, nutritional solutions, blood products, and imaging solutions...
	Use of Fingerstick Devices on More Than One Person Poses Risk for Transmitting Bloodborne Pathogens: Initial Communication
	CDC and FDA have noted a progressive increase in the reports of bloodborne infection transmission over the past 10 to 15 years (primarily hepatitis B virus), resulting from the shared use of fingerstick and POC blood testing devices...
	Federal Register: Effective Date of Requirement for Premarket Approval for Four Class III Preamendments Devices
	The FDA is proposing to require the filing of a PMA or a PDP for the following four class III preamendments devices: Ventricular bypass (assist) device; pacemaker repair or replacement material; female condom; and transilluminator for breast evaluation.
	Federal Register: Food and Drug Administration Clinical Trial Requirements, Regulations, Compliance, and Good Clinical Practice; Public Workshop
	The public workshop on FDA's clinical trial requirements is designed to aid the clinical research professional's understanding of the mission, responsibilities, and authority of FDA and to facilitate interaction with FDA representatives. The program will
	Guidance for Industry and Food and Drug Administration Staff - Contact Lens Care Products Labeling
	This guidance document is an addendum to a special control guidance that supports the classification of the Contact Lens Care Products as class II (special controls). This draft guidance will be issued in conjunction with a Federal Register notice...
	Guidance for Industry and Food and Drug Administration Staff - Guidance for the Non-Clinical and Clinical Investigation of Devices Used for the Treatment of Benign Prostatic Hyperplasia (BPH)
	As men age, the prostate enlarges over time obstructing the prostatic urethra and interfering with sphincter function. The resulting condition, known as benign prostatic hyperplasia (BPH), is associated with decreased peak urinary flow rate...
	Class I Medical Device Recall: Ikaria Holdings, INOMAX DS Drug Delivery System
	Reason for Recall: A component within the pressure switch, which monitors when the drug supply should be replaced, may tear. Risks to the patient may include interruption of drug flow due to an empty cylinder, and/or the time taken to switch to a...
	PMA Final Decisions for July 2010
	These are Premarket Approvals (PMA), Product Development Protocols (PDP), Supplement and Notice Decisions for July 2010.
	Public Workshop - Medical Devices and Nanotechnology: Manufacturing, Characterization, and Biocompatibility Considerations, September 23, 2010
	The purpose of this workshop is to obtain information on the safety and effectiveness of medical devices utilizing nanotechnology. Specifically, FDA would like public input on manufacturing, characterization, and biocompatibility evaluation of medical...
	Federal Register: Public Workshop on Medical Devices and Nanotechnology: Manufacturing, Characterization, and Biocompatibility Considerations
	The purpose of this workshop is to obtain information on manufacturing, characterization, and biocompatibility evaluation of medical devices containing or utilizing nanomaterials and nanostructures, including diagnostics. FDA is seeking input on these...
	Federal Register: ASK (Assess Specific Kinds of CHILDREN Challenges for Neurologic Devices) Study Children Workshop; Public Workshop; Request for Comments
	The purpose of the public workshop is to solicit comments from academic investigators and clinicians associated with the use, research and/or development of pediatric neuroprostheses regarding approaches for enhancing the protection and promotion of...
	FDA Safety Notification: Mammography Problems at Med Pro Imaging in Plantation, Florida
	The FDA has become aware of problems associated with the quality of mammograms performed at the Med Pro Imaging facility, formerly located at the following address: 7050 NW 4th Street, Suite #202, Plantation, Fla. 33317. Med Pro is under new management...
	FDA Safety Notification: Ultraviolet Radiation Over-Exposure from Tootsie Tanner, a Portable Foot Tanning Device
	The Tootsie Tanner, a portable foot tanning device, is labeled with an improper exposure schedule and has an inadequate timer control, each of which could lead to an overdose of ultraviolet radiation. The labeled exposure schedule indicates the product...
	Public Workshop - ASK CHILDREN (Assess Specific Kinds of CHILDREN Challenges for Neurologic Devices) STUDY Workshop, September 13, 2010
	The FDA is announcing a public Workshop to solicit information from academic investigators and clinicians associated with the use, research and/or development of pediatric neuroprostheses regarding approaches for enhancing the protection and promotion...
	Public Workshop - Medical Device User Fee Program Public Meeting, September 14, 2010
	The FDA is is announcing a public meeting on the reauthorization of the medical device user fee program. The current legislative authority for the medical device user fee program expires in September 2012 and new legislation will be required for FDA...
	Federal Register: Oversight of Laboratory Developed Tests; Public Meeting; Reopening of the Comment Period
	The FDA is reopening until September 15, 2010, the comment period for the notice that published in the Federal Register of Thursday, June 17, 2010 (75 FR 34463).
	Federal Register: General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting; Meeting on November 18, 2010
	This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public. Name of Committee: General and Plastic Surgery Devices Panel of the Medical Devices Advisory...
	Federal Register: Medical Device User Fee Act; Public Meeting; Request for Comments; Meeting on September 14, 2010
	The FDA is announcing a public meeting on the reauthorization of the medical device user fee program. The current legislative authority for the medical device user fee program expires in September 2012 and new legislation will be required for FDA to...
	Class I Medical Device Recall: St. Jude Medical 6 French Engage? Introducer Devices
	The Company identified that some devices in the affected batches have the potential for separation of the shaft (sheath) from the hub or for a break in the hub assembly. If either of these were to occur during use, a potentially life threatening...
	Positive Displacement Needleless Connectors and Bloodstream Infections: Initial Communication
	Several peer-reviewed clinical studies report an increase in bloodstream infections following the introduction and use of positive displacement needleless connectors in healthcare facilities, as well as a reduction in infections after changing to another
	Federal Register: Comprehensive List of Guidance Documents at the Food and Drug Administration; Notice
	The FDA is publishing a comprehensive list of all guidance documents currently in use at the agency. This list is being published under FDA's GGPs. It is intended to inform the public of the existence and availability of all of our current guidance...
	Public Workshop - Optimizing Clinical Trial Design for the Development of Pediatric Cardiovascular Devices, September 30th, 2010
	Rarely have devices been developed, evaluated and approved specifically for treatment of children with congenital heart disease. The small, heterogeneous population, need for long-term follow-up, lack of market incentive, and misperceptions of...
	Removing Retrievable Inferior Vena Cava Filters: Initial Communication
	IVC filter usage has increased rapidly during the past thirty years. In 1979, 2,000 IVC filters were used, while in 2007, almost 167,000 filters were implanted, and the market for IVC filters is only expected to increase, with an estimated 259,000 IVC...
	Safety Investigation of Suspected Counterfeit Combat Application Tourniquets (C-A-T®): Initial Communication
	FDA has become aware of suspected counterfeit C-A-T ® tourniquets. The suspected counterfeit tourniquets have subtle differences in stitching, printing of the logo and molding of plastic parts. They may be packaged and labeled for a distributor other than
	Federal Register: Workshop on Optimizing Clinical Trial Design for the Development of Pediatric Cardiovascular Devices
	The topic to be discussed is pediatric cardiovascular device development. The purpose of the public workshop is to solicit information from clinicians, academia, professional societies, other government agencies, and industry on various efficient and...
FDA News
	FDA cautions consumers about Estrella Family Creamery cheeses
	The U.S. Food and Drug Administration is warning consumers to discard cheeses from Estrella Family Creamery of Montesano, Wash., because they may be contaminated with Listeria monocytogenes. Environmental samples and one product sample collected by the FDA during an August 2010 inspection at the facility have tested positive for L. mono.
	FDA seeks court order against Michigan dairy
	The U.S. Department of Justice, on behalf of the U.S. Food and Drug Administration, has filed a complaint for permanent injunction against Scenic View Dairy of Hamilton, Mich., its president, and three of its managers alleging that they sold dairy cows for human consumption that contained illegal drug residues in edible tissues.
	FDA launches new organizational performance management system
	The U.S. Food and Drug Administration today launched an innovative performance management system designed to advance the President?s commitment to transparency, public participation, and collaboration in the work of government.
	FDA Warns Consumers to Avoid TimeOut Capsules
	The U.S. Food and Drug Administration is warning consumers not to take TimeOut Capsules because it contains an active drug ingredient that can dangerously lower blood pressure. The product is marketed as a dietary supplement for sexual enhancement.
	FDA releases guidance on federal menu labeling requirements
	The U.S. Food and Drug Administration today released two documents that outline steps to help chain restaurants comply with new federal nutrition labeling requirements.
	FDA Warns of Possible Dangers from Portable Foot-Tanning Device
	The U.S. Food and Drug Administration is warning consumers about the risk of ultraviolet radiation overdose with the Tootsie Tanner portable foot tanning device.
	Study: Presence of murine leukemia virus found in CFS Patients, others
	Researchers have found murine leukemia viruses (MLV) in blood samples collected from patients diagnosed with chronic fatigue syndrome (CFS) and some healthy blood donors, according to a study published online today by the scientific journal Proceedings of the National Academy of Sciences (PNAS).
	Urgent Nationwide Egg Recall
	The current recall of eggs in their shells, or ?shell eggs,? is part of an ongoing and intensive investigation by local, state, and federal officials into the cause of recent cases of Salmonella Enteritidis.
	Urgent Nationwide Frozen Mamey Fruit Products Recall
	An investigation by the CDC and state partners showed an epidemiologic link between an ongoing outbreak of Salmonella Typhi and frozen mamey fruit products sold under the La Nuestra brand by Montalvan Sales Inc. Ontario, Calif, and under the Goya brand by Goya Foods Inc. Secaucus, New Jersey.
	U.S. Marshals seize food from rodent-infested Ga. warehouse
	U.S. Marshals, acting under a court order sought by the U.S. Food and Drug Administration, today seized packaged food products from a rodent-infested warehouse in Athens, Ga. A variety of products, including crackers, cookies and potato chips, were intended for sale to jails and prisons throughout the southeastern United States.
	FDA Proposes Withdrawal of Low Blood Pressure Drug
	The U.S. Food and Drug Administration today proposed to withdraw approval of the drug midodrine hydrochloride, used to treat the low blood pressure condition orthostatic hypotension, because required post-approval studies that verify the clinical benefit of the drug have not been done.
	FDA approves ella? tablets for prescription emergency contraception
	The U.S. Food and Drug Administration today approved ella? (ulipristal acetate) tablets for emergency contraception. The prescription-only product prevents pregnancy when taken orally within 120 hours (five days) after a contraceptive failure or unprotected intercourse. It is not intended for routine use as a contraceptive.
	FDA: Aseptic Meningitis Risk with Use of Seizure Drug Lamictal
	The U.S. Food and Drug Administration today warned that the drug Lamictal (lamotrigine), approved to treat seizures and bipolar disorder, can cause aseptic meningitis, an inflammation of the protective membranes (meninges) that cover the brain and spinal cord not caused by bacterial infection.
	FDA: Salmonella risk from frozen rodents fed to reptiles
	The U.S. Food and Drug Administration is warning U.S. and international customers who may have purchased frozen mice, rats and chicks from Biggers and Callaham LLC, dba/MiceDirect.com, that these products, which are used as food for reptiles, have the potential to be contaminated with Salmonella.
	FDA Seeks Injunction Against Colorado Manufacturer of Cultured Cell Product
	The U.S. Food and Drug Administration is seeking an injunction in federal court against Regenerative Sciences LLC, of Broomfield, Colo., citing violations of current good manufacturing practice (cGMP) that cause its cultured cell product to be adulterated. The product is also misbranded due to the lack of adequate directions for use and the failure to bear the ?Rx only? symbol.
	FDA Issues Assessments of the 510(k) Program and Use of Science in Decision-Making
	The U.S. Food and Drug Administration today issued two comprehensive evaluations containing recommendations that address three key objectives of the agency?s public health mission as it relates to medical devices ? foster device innovation, create a more predictable regulatory environment, and enhance device safety.
	Statement by Margaret A. Hamburg, Commissioner of Food and Drugs on the Reopening of Florida State Waters to Commercial Fishing
	We are pleased to be able to support the state of Florida as it reopens state waters off Pensacola to commercial fishing. Through close coordination with our state and federal partners, we are confident all appropriate steps have been taken to ensure that seafood harvested from the waters being opened today is safe and that Gulf seafood lovers everywhere can be confident eating and enjoying the fish that will be coming out of this area.
	Statement by Margaret A. Hamburg, Commissioner of Food and Drugs, on the Reopening of Some Mississippi State Waters to Commercial Fishing
	We are pleased to be able to support the state of Mississippi as it reopens state waters in the Mississippi Sound, from the mainland to the barrier islands, to commercial fishing. Through close coordination with our state and federal partners, we are confident all appropriate steps have been taken to ensure that seafood harvested from the waters being opened today is safe and that Gulf seafood lovers everywhere can be confident eating and enjoying the fish and shrimp that will be coming out of this area.?
	United States Seeks Permanent Injunction Against New York Food Processor
	The U.S. Department of Justice, in an action initiated by the U.S. Food and Drug Administration, is seeking a permanent injunction against NY Gourmet Salads, Inc., a processor of ready-to-eat deli salads, seafood salads, and cream cheeses in Brooklyn, N.Y., and Leonard F. Spada, the company's president. (HR)
	FDA Warns Consumers of Serious Harm from Drinking Miracle Mineral Solution (MMS)
	The U.S. Food and Drug Administration is warning consumers not to take Miracle Mineral Solution, an oral liquid also known as ?Miracle Mineral Supplement? or ?MMS.? The product, when used as directed, produces an industrial bleach that can cause serious harm to health.
FDA Recalls
	Sparboe Farms Provides Clarification on its Voluntary Recall of Fresh Shell Eggs
	Sparboe Farms issued the following clarification regarding the previously announced recall of shell eggs supplied by Wright County Egg and Hillandale Farms. One additional brand is linked to this recall associated with possible Salmonella contamination.
	The Hartz Mountain Corporation Recalls Hartz Naturals Real Beef Treats Because of Possible Salmonella Health Risk
	The Hartz Mountain Corporation is voluntarily recalling one specific lot of Hartz Naturals Real Beef Treats for Dogs due to concerns that one or more bags within the lot may have been potentially contaminated with Salmonella. Hartz is fully cooperating with the US Food and Drug Administration in this voluntary recall.
	Real Taste Noodle Manufacture Recalls Egg Noodle Because of Possible Health Risk
	Real Taste Noodle Manufacture of Chicago, IL is recalling bags of Egg Noodle (5lbs per bag, 10 bags per case), because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
	Cibo Vita issues Allergy Alert on Undeclared Sulfites in Mediterranean Mix of Woodpecker Brand
	Cibo Vita, 280 N. Midland Ave Saddle Brook, NJ 07663 is recalling Mediterranean Mix of Woodpecker brand because it may contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product. The recalled Mediterranean Mix, in plastic containers of 8.5 OZ was sold to the list of the attached customers.
	Good Taste Noodle MFG Recalls "Egg Noodles and Wonton Skins" Because Of Possible Health Risk
	Good Taste Noodle MFG. of Chicago, IL, is recalling its ?EGG NOODLES and WONTON SKINS, labeled with production date from June 19, 2010 to August 19, 2010?, because they have the potential to be contaminated with salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune system. Healthy persons infected with salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.
	Whole Foods Market® Announces Recall of Morningland Dairy and Ozark Hills Farm Cheese
	The following press release was issued by Whole Foods Market's North Atlantic Region regarding the voluntary recall of Morningland Dairy of Mountain View, Missouri, Raw Goat Milk Mild Cheddar Cheese. Whole Foods Market?s North Atlantic region is announcing a voluntary recall Morningland Dairy and Ozark Hills Farm Raw Goat Milk Mild Cheddar Cheese due to possible contamination by Listeria and Staphylococcus aureus.
	Azteca Linda Corp. Expands Recall of Queso Fresco Because of Possible Health Risk
	Azteca Linda Corp. of Brooklyn, NY, is expanding the 8/24/10 recall of QUESO FRESCO (FRESH WHITE CHEESE (exp. SEP 11 2010) to include expiration date SEP 12 2010. In addition, the firm is recalling Queso El Azteca brand REQUESON (RICOTTA CHEESE) with expiration date SEP 19 2010 because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems...
	P&G Voluntarily Recalls a Small Amount of Dry Cat Food
	CINCINNATI, August 31, 2010 - The Procter & Gamble Company (P&G) is voluntarily recalling a small number of bags from a specific lot of one of its dry cat food products due to potential salmonella exposure.
	QUESERIA CHIPILO INC. Recalls Cheese Products because of Possible Health Risk
	August 26, 2010 QUESERIA CHIPILO INC. is announcing a recall of the following cheese products, all date codes up to and including September 26, 2010 ? Fresco and Nov 25, 2010 ? Oaxaca.
	Torn & Glasser Issues Allergy Alert on Undeclared Peanuts Fancy, No Peanuts
	Torn & Glasser of Rancho Dominguez, CA is recalling its 3.75lb (#10) cans of ?Mixed Nuts Fancy, No Peanuts? marked with lot numbers 0980 and 1940 on the outer case label and bottom lid due to undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products. The recalled ?Mixed Nuts Fancy, No Peanuts? were distributed in CA, WA and HI. This was distributed through a wholesale distribution outlet. The product comes in a sealed, 3.75lb #10 style can marked with lot numbers 0980 and 1940 on the outer case label and bottom lid. The UPC is 072488980761.
	Paleta California Co. Announces Voluntary Recall of Frozen Mamey Paletas Because of Potential Contamination with Salmonella Typhi
	In response to the voluntary recall by Goya Foods, Inc. of their frozen mamey pulp, Paleta California, Co. is voluntarily recalling its 4 oz. Mamey Supreme Cream Bar (frozen fruit bars also known as ?paletas?) due to a potential health risk from Salmonella Typhi. Salmonella Typhi is a bacterium that causes a life-threatening illness called typhoid fever.
	Morningland Dairy Conducting Nationwide Voluntary Recall of All Cheese Labeled as Morningland Dairy & Ozark Hills Farm Because of Possible Health Risk
	Morningland Dairy of Mountain View, Missouri, is recalling 68,957 pounds of cheese because it may be contaminated with Listeria monocytogene and also has the potential to be contaminated with Staphylococcus aureus.Morningland Dairy?s raw milk cheese is sold in the lower 48 states via mail order, retail stores, crop sharing associations, and direct delivery. The cheese is packaged in vacuum-sealed plastic packages that are sold as random weight size retail packages. The specific varieties of cheese are sold under the following brand names and flavors:
	P&G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado
	CINCINNATI, August 29, 2010 -- Procter & Gamble (P&G) is voluntarily recalling a small number of bags of its Iams Proactive Health Indoor Weight & Hairball Care dry cat food which may have been sold recently in one or two stores in Loveland, Colorado.
	Sparboe Farms Initiated Voluntary Recall Fresh Shell Eggs
	Sparboe Farms is voluntarily recalling shell eggs produced by Wright County Egg and Hillandale Farms which were packaged by Sparboe Farms, because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis, or arthritis.
	Queseria Chipilo Recalls Cheese Products Because of Possible Health Risk
	Queseria Chipilo , Passaic, NJ is announcing to recall of the following cheese products, all date codes up to and including Sept. 26, 2010 Fresco and Nov. 25,2010 Oaxaca.Oaxaca String Cheese Queso Fresco . Queso Fresco. Hoja De Plátano
	Fruiti Pops, Inc. Recalls "Fruiti Pops" Brand Mamey Frozen Fruit Bars Because of Potential Health Risk
	In response to the voluntary recall of Goya Foods, Inc. frozen mamey pulp, Fruiti Pops, Inc. of Santa Fe Springs, CA is recalling its Fruiti Pops 4 oz. Mamey frozen fruit bars due to a potential health risk from Salmonella typhi. No illnesses have been reported to date in connection with Fruiti Pops Mamey fruit bars.
	Cal-Maine Foods, Inc. Clarifies Previous Statement on Nationwide Shell Egg Recall
	Cal-Maine Foods, Inc. (NASDAQ: CALM) today issued the following clarification regarding the previously announced voluntary recall of shell eggs supplied from Hillandale Farms of Iowa. This information does not increase the total number of eggs which Cal-Maine purchased from Hillandale Farms, which was previously announced on August 20, 2010. Cal-Maine immediately contacted its customers to ensure that any eggs included in the recall were withdrawn from the marketplace.
	Cardenas Market Brand Label Included in Wright County Egg Recall
	The following statement was released by officials of Wright County Egg regarding its voluntary recall of some shell eggs in cooperation with the US Food and Drug Administration's (FDA). Wright County Egg of Galt, Iowa is adding one California-distributed brand label ? Cardenas Market ? to its voluntary recall of August 13, 2010 of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella...
	Trafficanda Egg Ranch Initiates Voluntary Recall of Medium, Large, X Large, & Jumbo AA Cartons; 5 Dozen Medium Over Wrap & 20 Count Over Wrap, Fresh Shell Eggs Because of Possible Health Risk
	The following statement was released by officials of Trafficanda Egg Ranch regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa and distributed by Trafficanda Egg Ranch. Trafficanda Egg Ranch is voluntarily recalling specific Julian dates of Medium, Large, X Large, and Jumbo Cartons; 5 Dozen Medium Over Wrap and 20 Count Over Wrap of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with Salmonella...
	Azteca Linda Corp. Recalls Queso Fresco and Queso Hebra because of Possible Health Risk
	Azteca Linda Corp. of Brooklyn, NY, is recalling QUESO FRESCO (FRESH WHITE CHEESE) and QUESO HEBRA (FRESH WHITE STRING CHEESE) with an expiration date of September 11, 2010 because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.