Complete FDA and NHTSA recall records dated in May 2014.
These records include useful source details for the selected month.
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…
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…
Presence of Particulate Matter: During a review of retain samples, the firm found a glass particulate in one lot of Acetylcysteine Solution
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
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…
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Failed Dissolution Specifications: One lot of product is being voluntarily recalled because dissolution test results failed to meet specification throughout the product's shelf life.
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Marketed Without An Approved NDA/ANDA: Product is being recalled due to excessive levels of lovastatin. Lovastatin is an FDA approved drug making this dietary supplement an unapproved new…
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Presence of Foreign Tablets: Presence of atenolol 25 mg tablet mixed into promethazine 25 mg tablet bottles.
The contract manufacturer has notified Swanson Health Products that Swanson Full Spectrum Cilantro (Coriander) (SW1112) is subject to a recall due to a potential risk of salmonella…
IEH sample had positive result for Listeria Monocytogenes of Purity Brand Organic Fresh Mango.
Fernandez Chile Company is recalling 4oz Chile Molido Puro medium hot UPC 77601-10011 and 6oz Chile Rojo mild UPC 77601-10053 due to contamination with Salmonella.
The firm discovered that the label for two of their products did not declare eggs in the ingredient statement.
Fernandez Chile Company is recalling 4oz Chile Molido Puro medium hot UPC 77601-10011 and 6oz Chile Rojo mild UPC 77601-10053 due to contamination with Salmonella.
The firm discovered that the label for two of their products did not declare eggs in the ingredient statement.
Product labeling on Trader Giotto's Caesar Salad with Caesar Dressing may not list wheat, soy, egg and fish (anchovy) allergens.
Soy Bean Cake products do not declare wheat, a sub ingredient of soy sauce.
Product was found to be contaminated with Listeria monocytogenes
The product contained undeclared sulfites (440 ppm), undeclared FD&C Yellow # 6, and unapproved color Ponceau 4R, based on sampling and analysis by New York State Department of Agriculture…
Labeling: Label Error on Declared Strength; Listed active ingredient strength is inaccurate.
Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the counter whose labeling indicates it is to be used for the treatment of disease.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
