Health Recalls
This is a list of health recalls. These recalls are listed with the most recent first.
-
-
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.
-
-
-
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.
-
-
-
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.
-
-
-
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 “paletasâ€) due to a potential health risk from Salmonella Typhi. Salmonella Typhi is a bacterium that causes a life-threatening illness called typhoid fever.
-
-
-
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 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.
-
-
-
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.
-
-
-
The magnetic maze board's plastic wand can separate and expose a magnet that can be a choking hazard to children. Also, if a child has more than one of these toys and the magnets detach and are swallowed, the magnets can attract each other and cause intestinal perforations or blockages, which can be fatal.
-
-
-
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...
-
-
-
Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter. There were a total of 1,924 units distributed, 258 in the United States of America 1,586 in the European Union and 80 in countries. A total of eight (8) complaints regarding the inflation or deflation of the NeuroBalloon Catheter were received by Integra. All complaints occurred outside the United States. No patient injuries have been reported. As a result of the investigation performed by Integra, it was determined that this condition could exist during pre-implant testing or during the procedure. Integra issued a voluntary recall of the affected lots of the NeuroBalloon Catheter on July 2, 2010.
-
-
-
When the temperature setting is in "low," the smoker's hose/valve/regulator (HVR) assembly does not allow sufficient gas to flow, causing the flame to extinguish. Gas continues to flow and build up inside the smoker. If the smoker is reignited the build-up of propane gas can cause an explosion that bursts the smoker's door open, posing an injury hazard.
-
-
-
Natural Wellness is announcing that it is conducting a nationwide voluntary recall of MasXtreme, Lot # 907043, UPC 094922300805. Laboratory analysis conducted by FDA has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil...
-
-
-
NY Fish Inc, 738 Chester St, Brooklyn, NY, 11236 is recalling NY Fish Brand (cold) Smoked Herring, with a code of 141, discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection. The product was found to be uneviscerated prior to processing.
-
-
-
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Snow White Food Products Inc., located in 621 Bergen Street in Brooklyn, New York, is recalling certain packages of "Alfalfa Sprouts" due to the presence of Salmonella. The recalled "Alfalfa Sprouts" is packaged in a 3.5 ounce plastic clamshell container which is uncoded. It has a UPC code of 0-46421-11236-6. The product was distributed in New York State.
-
-
-
Milton's Baking Company is voluntarily recalling Milton's Multi-Grain Bread which was distributed to locations in Northern and Central California, Arizona and Nevada. The company took the precautionary step because the loaves contain milk, an undeclared allergen, which may pose a potential serious and life-threatening health risk to milk-allergic individuals.
-
-
-
AustiNuts Wholesale, Inc. is issuing this voluntary recall of pistachio kernel products due to a recall that was issued by it's supplier California Delights, Inc. California Delights, Inc issued a recall for two shipments of pistachio kernels received by AustiNuts Wholesale, Inc. in July 2010 due to the possibility of contamination with Salmonella.
-
-
-
J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement Lot 6032101 distributed by the company was found to contain undeclared Desmethyl Sibutramine, similar in structure to Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved Slim-30 Herbal Supplement, therefore the safety and effectiveness of the product is unknown.
-
-
-
Elie Baking Corp. dba Near East Baking Corporation, 204 N Montello St,, Brockton, Massachusetts is recalling the following: Food City brand, Low Carb Tortilla White, 13.5 oz, 10 count. UPC 0 87848 42002 0
Food City brand, Low Carb Tortilla Whole Wheat, 13.5 oz.10 count. UPC 0 87848 42003 0
MFG Date 07/21/10 & MFG Date 07/22/10 stamped on the top left of the bag.
-
-
-
While the actual electrical wire has "14 gauge" printed on it, the packaging incorrectly labels the electrical wire as 12 gauge. If used as a 12 gauge wire, it can overload, posing a fire hazard to consumers.
-
-
-
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Sunny Lake Trading Inc, located at 651A Lexington Ave, Brooklyn, New York is recalling "Golden Bridge" dried dates due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
-
-
-
Glow Industries, Inc., Perrysburg, OH, announced today that it is initiating a voluntary nationwide recall of the company's product sold under the name of Mr. Magic Male Enhancer from Don Wands. Glow Industries, Inc. is conducting this voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found the Mr. Magic Male Enhancer from Don Wands capsules to contain Hydroxythiohomosildenafil and Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making Mr. Magic Male Enhancer an unapproved new drug. These active ingredients are not listed on the product label. Product manufactured containing lot numbers 9041401, 251209 and 8121904 are included in this recall...
-
-
-
Moonstruck Chocolate Co. of Portland, Oregon is voluntarily recalling their 4 piece Cream Cone Chocolate Truffle Collection and the 12 piece Chocolate Malted (or Malt) Cream Cone Chocolate Truffles, because they may contain undeclared peanut butter. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.
-
-
-
Kroger
(product distributor) and Contessa Premium Foods, Inc. (product manufacturer) are recalling 24
ounce bags of Kroger brand Meals Made Simple Shrimp Linguini, because it may contain
undeclared milk product. People who have an allergy or severe sensitivity to milk products run
the risk of serious or life-threatening allergic reaction if they consume this product.
-
-
-
New York State Agriculture Commissioner Patrick Hooker today warned consumers in the Queens County, New York area not to consume certain “Queso Cotija Cheese†made by Mexicali Cheese Corp, 91-52 87th Street, Woodhaven, New York 11421 due to possible Staphylococcus aureus contamination.
-
-
-
Strong America Ltd. of Long Island City, NY is recalling Golden Smell brand "Dried Potato" packages with code DB35/TI02.7-2001 because they contain undeclared sulfites. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reaction if they consume this product.
-
-
-
Goya Foods, Inc. of Secaucus, NJ, is recalling its 14 ounce packages of Frozen Mamey Pulp,
due to a potential health risk from Salmonella. No illnesses have been reported to date in
connection with Goya brand Mamey Pulp.
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.
-
-
-
Salt Lake City, UT announced today that it is conducting a voluntary nationwide recall of the company’s product sold under the name Prolatis’. Prolatis’ is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found Prolatis’ to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making Prolatis’ an unapproved drug. The active drug ingredient is not listed on the product label. Product manufactured prior to August 9, 2010 is included in this recall. Prolatis’ is sold nationwide in double blister packs and 40 count bottles.
-
-
-
Novacare LLC announced today that it is conducting a voluntary nationwide recall of products sold under the following names: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, and Zilex (with Golden Spear).
Novacare LLC has been informed by representatives of the Food & Drug Administration (FDA) that the products appear to contain sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction.
-
-
-
Ikaria, Inc. announced today that its INOMAX® DS drug-delivery systems in
the United States are being voluntarily recalled due to the potential failure of a pressure switch which may
have an impact on the administration of INOMAX® (nitric oxide) for inhalation to patients. This potential
failure was identified by Ikaria as part of its ongoing quality monitoring and review processes. This class I
recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).
-
-
-
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the US Food and Drug Administration (FDA) that FDA lab analysis of Revivexxx® Extra Strength distributed by the company was found to contain undeclared tadalafil. Tadalafil is an FDA-approved drug for the treatment of male Erectile Dysfunction (ED), making Revivexxx® Extra Strength an unapproved drug.
-
-
-
EZVille, Ltd. of Ronkonkoma, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Solo Slim® distributed by the company was found to contain an undeclared drug ingredient. Solo Slim® was found to contain Didesmethyl Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved Solo Slim®, therefore the safety and effectiveness of the product is unknown.
-
-
-
The South Bend Chocolate Company, South Bend, Indiana, is recalling 174 1-lb bags of Bountiful Blend, a blend of chocolate covered mixed nuts and dried fruits, because it contains undeclared cashews, almonds, pecans, and Brazil nuts. People who have an allergy or severe sensitivity to cashews, pecans, almonds or Brazil nuts run the risk of serious or life-threatening allergic reaction if they consume this product.
-
Note: Our database contains safety recalls issued by the Consumer Product Safety Commission (CPSC), the National Highway Traffic Safety Administration (NHTSA) and the Food and Drug Administration (FDA). For a complete release on alerts, recalls, or press releases issued to the public please visit the appropriate website. A compiled list of these websites can be found in the links section of this website.
Disclaimer: This information presented on this website is being provided as a courtesy. We've worked really hard to keep the records in our database as current and accurate as possible. In the unlikely event that our automated system fails, or contains bugs that incur incomplete records we take no responsibility. We take no responsibility for the information presented on this website. For a complete release on recalled products please visit the appropriate websites.