FoodMay 28, 2014
Stonyfield YoBaby Pear/Peach Organic Whole Milk Yogurt recall — FDA F-1954-2014
Product has elevated levels of coliforms
Class IIFDA: TerminatedStonyfield Farm
Monthly breakdown
2014 recalls by month
Select a month to review the recall records reported during that period.
December 2014206 records · 2 categoriesNovember 2014617 records · 2 categoriesOctober 2014159 records · 2 categoriesSeptember 2014101 records · 2 categoriesAugust 2014118 records · 2 categoriesJuly 2014224 records · 3 categoriesJune 201483 records · 2 categoriesMay 2014120 records · 2 categoriesApril 2014219 records · 2 categoriesMarch 2014137 records · 2 categoriesFebruary 201484 records · 2 categories
2014 recalls — page 64
Records are ordered by the best available source date.
FoodMay 28, 2014
J. R. Simplot Co. Corporate HQ PDP reads in part "***GOOD FOOD MADE SIMPLE***breakfast in a recall — FDA F-1968-2014
Raw material supplier accidently added sodium benzoate to the salsa used in manufacturing the finished product. Sodium benzoate was not declared on the ingredient statement of both the raw…
Class IIIFDA: TerminatedJ. R. Simplot Co. Corporate HQ
FoodMay 28, 2014
Harvest Sensations Verdex Fresh Snow Peas packed in 10 pounds cartons, keep recall — FDA F-1927-2014
Unapproved fungicide residue detected on random sample. Carbendizam at 28 ppb
Class IIIFDA: TerminatedHarvest Sensations LLC
FoodMay 28, 2014
Aqua Filter Fresh Inc., Pittsburgh, PA 15239 Permit #504 Source: Plum Boro recall — FDA F-1950-2014
For Spring Water and Purified Water bottled 4/17 - 18/2014, Outside lab results were positive for Coliforms and non-speciated E. coli.
Class IIFDA: TerminatedAqua Filter Fresh, Inc.
FoodMay 28, 2014
Stonyfield YoToddler Raspberry/Pear Cereal Organic Whole Milk recall — FDA F-1956-2014
Product has elevated levels of coliforms
Class IIFDA: TerminatedStonyfield Farm
FoodMay 28, 2014
Pepsi Beverages Company Lipton Pure Leaf Iced NTS Honey Green Tea 12 Pack recall — FDA F-1966-2014
Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products produced on March 3, 4, 5, and 6th of 2014 due to recent consumer complaints regarding apparent mold in the…
Class IIFDA: TerminatedPepsi Beverages Company
FoodMay 28, 2014
H:20 Innovations Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz x 4 recall — FDA F-1953-2014
H:20 Innovations is recalling Meijer Brand Baby Pediatric Electrolyte Fruit and Strawberry Flavor 8oz drinks due to a seal defect found during a complaint investigation.
Class IIFDA: TerminatedH:20 Innovations LLC
FoodMay 28, 2014
Pepsi Beverages Company Lipton Pure Leaf Iced Tea Sweet Tea 18.5OZ PL 6 Pack recall — FDA F-1963-2014
Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products produced on March 3, 4, 5, and 6th of 2014 due to recent consumer complaints regarding apparent mold in the…
Class IIFDA: TerminatedPepsi Beverages Company
FoodMay 28, 2014
Pepsi Beverages Company Lipton Pure Leaf Iced NTS Peach Tea 12 Pack recall — FDA F-1967-2014
Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products produced on March 3, 4, 5, and 6th of 2014 due to recent consumer complaints regarding apparent mold in the…
Class IIFDA: TerminatedPepsi Beverages Company
FoodMay 28, 2014
Pepsi Beverages Company Lipton Pure Leaf Iced Tea Lemon 18.5OZ PL 12 Pack recall — FDA F-1965-2014
Pepsi Co has announced a recall of some Lipton Pure Leaf Iced Tea products produced on March 3, 4, 5, and 6th of 2014 due to recent consumer complaints regarding apparent mold in the…
Class IIFDA: TerminatedPepsi Beverages Company
FoodMay 28, 2014
H:20 Innovations Meijer Baby Pediatric Electrolyte Fruit Flavor 8oz x 4 with recall — FDA F-1952-2014
H:20 Innovations is recalling Meijer Brand Baby Pediatric Electrolyte Fruit and Strawberry Flavor 8oz drinks due to a seal defect found during a complaint investigation.
Class IIFDA: TerminatedH:20 Innovations LLC
DrugMay 28, 2014
Schindele Enterprises dba Midwest Wholesale MiracleZEN Platinum, 1 pill blister pack, 2000 recall — FDA D-1337-2014
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Class IFDA: TerminatedSchindele Enterprises dba Midwest Wholesale
DrugMay 28, 2014
Herbal Give Care Esbelder Man Herbal Blend With L-Carnitine Dietary Supplement, 30 capsule recall — FDA D-1332-2014
Marketed Without an Approved NDA/ANDA: Products found to contain undeclared sibutramine, N-Desmethylsibutramine, and N-di- Desmethylsibutramine. Sibutramine was removed from the U.S. market…
Class IFDA: TerminatedHerbal Give Care LLC
DrugMay 28, 2014
Herbal Give Care Esbelder Fem Mezcla con L-Carnitina Suplemento Alimenticio,30 capsule recall — FDA D-1333-2014
Marketed Without an Approved NDA/ANDA: Products found to contain undeclared sibutramine, N-Desmethylsibutramine, and N-di- Desmethylsibutramine. Sibutramine was removed from the U.S. market…
Class IFDA: TerminatedHerbal Give Care LLC
DrugMay 28, 2014
Herbal Give Care Esbelin Siloutte Te, Suplemento Alimenticio, herbal tea in a gold recall — FDA D-1330-2014
Marketed Without an Approved NDA/ANDA: Products found to contain undeclared sibutramine, N-Desmethylsibutramine, and N-di- Desmethylsibutramine. Sibutramine was removed from the U.S. market…
Class IFDA: TerminatedHerbal Give Care LLC
DrugMay 28, 2014
Tendex NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5 recall — FDA D-1346-2014
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs.
Class IFDA: TerminatedTendex
DrugMay 28, 2014
Schindele Enterprises dba Midwest Wholesale Magic For Men recall — FDA D-1338-2014
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Class IFDA: TerminatedSchindele Enterprises dba Midwest Wholesale
DrugMay 28, 2014
Pfizer Us Pharmaceutical Group Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 recall — FDA D-1328-2014
Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of Effexor XR 150 mg capsules contained a single peach colored capsule printed TKN250 which was identified as a…
Class IFDA: TerminatedPfizer Us Pharmaceutical Group
DrugMay 28, 2014
Liothyronine Sodium Tablets, USP 5 mcg recall — FDA D-1344-2014
Cross Contamination with Other Products: Four lots of Liothyronine Sodium Tablets, USP 5 mcg are being recalled due to the finding of a potential carryover of trace amounts of a previously…
Class IIFDA: TerminatedSigmaPharm Laboratories LLC
DrugMay 28, 2014
Tendex P-BOOST Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5 recall — FDA D-1345-2014
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs.
Class IFDA: TerminatedTendex
DrugMay 28, 2014
Herbal Give Care Esbelin Siloutte Mezcal Herbal con L-Carnitine Suplemento Alimenticio, 30 recall — FDA D-1329-2014
Marketed Without an Approved NDA/ANDA: Products found to contain undeclared sibutramine, N-Desmethylsibutramine, and N-di- Desmethylsibutramine. Sibutramine was removed from the U.S. market…
Class IFDA: TerminatedHerbal Give Care LLC
DrugMay 28, 2014
Fresenius Medical Care Holdings phosLo (calcium acetate) GelCaps, 667 mg, 200-count bottle recall — FDA D-1343-2014
Cross Contamination with Other Products: Potential for contaminant on the cotton packaging inside the bottle. Chemical analysis of the contaminant found on the cotton was identified as a…
Class IIFDA: TerminatedFresenius Medical Care Holdings, Inc.
DrugMay 28, 2014
Ben Venue Laboratories Acetylcysteine Solution, USP, 10%, 30 mL vial recall — FDA D-1326-2014
Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution
Class IFDA: TerminatedBen Venue Laboratories Inc.
DrugMay 28, 2014
Schindele Enterprises dba Midwest Wholesale XZEN PLATINUM, 750 mg recall — FDA D-1340-2014
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Class IFDA: TerminatedSchindele Enterprises dba Midwest Wholesale
About the 2014 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.