Recent FDA & US Consumer Product Safety Commission Recalls
Currently Showing FDA Recall Notices
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Gel Spice Company, Inc. Issues A Voluntary Recall Of Fresh Finds Brand Ground Black Pepper, 3.53 oz (100 g), Due To Possible Salmonella Risk
Filed: Tuesday,September 16, 2014, 11:12 am
Gel Spice Company, Inc., of Bayonne, NJ, is issuing a voluntary recall notice for 16,443 cases of Fresh Finds-Ground Black Pepper, 3.53 oz, plastic jars, because it has the possibility 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.
Taylor Farms Pacific, Inc. voluntarily recalls Roma Tomatoes due to potential Salmonella contamination
Filed: Monday,September 15, 2014, 4:38 pm
Taylor Farms Pacific, Inc. of Tracy, CA has been notified that specific lots of “Expo Fresh” Roma tomatoes supplied to Taylor Farms Pacific may be contaminated with Salmonella as a result of routine testing. No illnesses have been reported.
Playtex Adds Production Lot To Its March 2014 Voluntary Recall Of Certain AC/DC Power Adapters Used With the Playtex® Nurser Deluxe Double Electric Breast Pump
Filed: Monday,September 15, 2014, 2:22 pm
Energizer Personal Care – Playtex Manufacturing, Inc. announced today that, out of an abundance of caution, it is adding an adapter production lot to its voluntary nationwide recall of certain AC/DC power adapters that are used with the Playtex® Nurser Deluxe Double Electric Breast Pump. No injuries have been reported to date.
Hospira Issues a Voluntary Nationwide Recall of One Lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), In 0.9 percent Sodium Chloride Injection, 500 Ml, Due to Particulate Matter
Filed: Thursday,September 11, 2014, 3:22 pm
LAKE FOREST, Ill., - Hospira, Inc. (NYSE: HSP), announced today it is initiating a voluntary nationwide user-level recall of one lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL, NDC 0409-7620-03 Lot 41-046-JT with expiration date of 01NOV 2015. This action is due to one confirmed customer report of particulate in a single unit.
Publix Recalls Private Label Jalapeno Bagels
Filed: Tuesday,September 9, 2014, 8:19 am
Out of an abundance of precaution, the company is issuing a voluntary recall for Publix Jalapeno Bagels, which are sold in either the self-service bins or artisan cases in the bakery department, and may contain pieces of glass and small stones.
The Publix Jalapeno Bagels were distributed to Publix store locations in Alabama, Florida, Georgia and South Carolina. Publix stores in Tennessee and North Carolina are not impacted by this recall.
Plum Organics Voluntarily Recalls Little Cremes Organic Rice Milk Snacks Due to Potential Choking Hazard
Filed: Monday,September 8, 2014, 2:20 pm
Plum Organics is voluntarily recalling its Little Cremes organic rice milk snacks line after it was found that the product has the potential to cause choking. The small, bite-sized snack pieces are made to soften in a child's mouth in less than 20 seconds making them easy to swallow.
Mars Chocolate North America Issues Allergy Alert Voluntary Recall on Undeclared Peanuts and Eggs in TWIXÂ® Bites 7oz Stand Up Pouch
Filed: Monday,September 8, 2014, 6:56 am
Today, Mars Chocolate North America announced a voluntary recall of its TWIXÂ® Brand Unwrapped Bites 7 oz. Stand Up Pouch with the code date: 421BA4GA60. Fewer than 25 cases of the stand-up pouches in this single lot code may contain product containing peanuts and eggs without listing them on the ingredient label.
Pharmacy Creations Issues Voluntary Recall of Four Product Lots With Limited Distribution in Florida, New Jersey, New York, and Puerto Rico Due to Potential Non-Sterility
Filed: Saturday,September 6, 2014, 11:42 am
Pharmacy Creations has voluntarily recalled four product lots (see below) following testing results conducted by Front Range, Inc., its former independent testing laboratory, that indicated that the product lots may have the potential of not being sterile. Pharmacy Creations no longer uses Front Range, Inc. for testing of any kind for any of its formulations.
Tullia’s Recalls Sauce Because of Possible Health Risk
Filed: Thursday,September 4, 2014, 1:00 pm
Tullia’s is recalling Italian Meatless Pasta Sauce code 530140. This recall has been initiated because a records review by the Washington State Department of Agriculture revealed that one batch of sauce produced with the 530140 code had a pH level high enough to allow the growth of Clostridium botulinum. If present, this organism can cause botulism, a serious and potentially fatal foodborne illness.
La Orocovena Biscuit Voluntarily Recalls Pound Cake de Queso Due to Undeclared Milk, Soy and Wheat
Filed: Wednesday,September 3, 2014, 1:46 pm
Through this means we inform to all La Orocoveña Biscuit clients that we will be conducting a recall of the product Pound Cake de Queso, 2oz. Exp. Dates 08/11/2014 to 10/12/2014, this since the product contains undeclared milk, wheat and soy.
Tjs Place recalls Basil Pesto Pasta because of potential health risk
Filed: Wednesday,September 3, 2014, 1:43 pm
Tjs Place of Kirkland Washington is voluntarily recalling approx. 20 containers of Basil Pesto Pasta packed in 8 oz plastic tubs because it has 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. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Martin Avenue Pharmacy, Inc. Issues a Voluntary Multi-State Recall of All Compounded Sterile Preparations Due to a Lack of Assurance of Sterility
Filed: Tuesday,September 2, 2014, 11:02 am
Naperville, Illinois, Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all in-date compounded sterile preparations. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.
PEDIGREE Adult Complete Nutrition Limited Recall Due to Metal Fragments (Expanded)
Filed: Monday,September 1, 2014, 12:47 pm
At PEDIGREE, we care about all dogs and their safety and well-being is extremely important to us, and to our mission - to make a Better World for Pets. For that reason, we have announced the extension of a previous voluntary recall of PEDIGREE Adult Complete Nutrition dry dog food products due to the possible presence of a foreign material.
4C Foods Corp. Voluntarily Recalls 4C Grated Cheese Homestyle Parmesan Because of Salmonella Contamination
Filed: Friday,August 29, 2014, 8:11 pm
4C Foods Corp. is recalling its 6-oz. glass jars of "4C Grated Cheese HomeStyle Parmesan", UPC 0-41387-32790-8 with code dates BEST BY JUL 21 2016 and JUL 22 2016 due to possible contamination with Salmonella. This recall does not impact any other 4C cheese products. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, elderly people, and others with weakened immune systems.
Regeneca Worldwide, a Division of Vivaceuticals, Inc Expands the Voluntarily Recall of Regeneslim Appetite Control Capsules Due to the Presence of DMAA that May Pose Possible Health Risk
Filed: Friday,August 29, 2014, 7:38 pm
Regeneca Worldwide a division of VivaCeuticals, Inc. Las Vegas, NV is expanding the voluntary nationwide recall of its RegeneSlim appetite control dietary supplement to include lot #823230415, lot #EX0616r 15813, Lot # EX0616R15814 and Lot #11414re5516 because FDA analysis confirmed the presence of DMAA. DMAA is also known as 1,3-dimethylamylamine, methylhexanamine, or geranium extract. DMAA is commonly used as a stimulant, pre-workout, and weight loss ingredient in dietary supplement products.
Solace International, Inc. Issues Voluntary Nationwide Recall of Dermatend Original and Dermatend Ultra Due to Safety Concerns
Filed: Friday,August 29, 2014, 7:28 pm
Reno, Nevada, Solace International, Inc. is voluntarily recalling all lots of Dermatend Original and Dermatend Ultra, in all sizes and dosage form, to the distributor/wholesaler level. A mole should be removed under the supervision of a dermatologist.
Kraft Foods Group Voluntarily Recalls Select Varieties of Regular Kraft American Singles Pasteurized Prepared Cheese Product Due to Ingredient Supplier's Out-of-Standard Storage Temperatures
Filed: Friday,August 29, 2014, 5:46 pm
Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties of regular Kraft American Singles Pasteurized Prepared Cheese Product. A supplier did not store an ingredient used in this product in accordance with Kraft’s temperature standards.
Dole Fresh Vegetables Announces Allergy Alert and Voluntary Limited Recall of DOLE-branded Spinach Due to Possible Contamination by Walnuts
Filed: Thursday,August 28, 2014, 7:09 pm
Although no illnesses or allergic reactions have been
reported, Dole Fresh Vegetables is initiating a limited voluntary recall of the following products:
This recall is due to possible contamination of these products by walnuts.
Mars Petcare US Announces Voluntary Recall of 22 Bags of PEDIGREE® Brand Adult Complete Nutrition for Dogs Sold at Dollar General in Mississippi, Arkansas, Tennessee and Louisiana
Filed: Wednesday,August 27, 2014, 12:02 pm
Today, Mars Petcare US announced a voluntary recall of 22 bags of PEDIGREE® Adult Complete Nutrition dry dog food products due to the possible presence of a foreign material. The bags were produced in one manufacturing facility, and shipped to one retail customer
UPDATED: CloverSnare 4-Loop Vascular Retrieval Snare Recall
Filed: Wednesday,August 27, 2014, 11:49 am
On July 10, 2014, Cook Medical initiated a recall of 696 of its CloverSnare™ 4-Loop Vascular Retrieval Snare devices. The device was recalled because of a potential for the loop to separate from the shaft, resulting in loss of device function, potential for embolization of snare fragments and the potential need for intervention to retrieve the separated snare.
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