Complete FDA and NHTSA recall records dated in June 2016.
These records include useful source details for the selected month.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Undeclared allergen; Peanut protein.
Undeclared allergens; wheat, soy and tree nuts (almonds).
The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do…
A positive result was discovered for Salmonella in Rose Red Filterbag Ginger and Organic Ground Ginger.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
The Clight brand products in flavors Orange, Lemon, Tangerine, and Lemon Tea contain a small amount of soy lecithin but are not labeled to declare soy lecithin in the ingredient list and do…
Undeclared allergen; Peanut protein.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Undeclared allergen; Peanut protein.
Undeclared allergen; Peanut protein.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Liquid Oil products were reported to contain a high density polyethylene resin trim ring in the 35 lb bottles.
Undeclared allergen; Peanut protein.
Potential contamination with Listeria monocytogenes.
Failed Impurities/Degradation Specifications: Par Pharmaceutical is recalling Pramipexole Dihydrochloride Extended Release tablets because it contains a known product impurity above…
Failed Dissolution Specifications
Labeling: Not Elsewhere Classified: correctly labeled bottles were packaged in cartons that were mislabeled with an incorrect active ingredient, phenylephrine rather than pseudoephedrine,…
Labeling: Wrong barcode. An incorrect bar code was noted on the vial label of Hectorol 2 mcg/1mL vial.
Failed Impurities/Degradation Specifications
Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot numbers are missing.
Failed Impurities/Degradation Specifications
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.
