WD IMPORT AND EXPORT Whole Dried Yellow Fish in bulk cardboard box, unlabeled recall — FDA F-1384-2016
The product was found to be uneviscerated based on sampling and analysis by New York State Department of Agriculture & Markets.
Complete FDA and NHTSA recall records dated in 2016, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
The product was found to be uneviscerated based on sampling and analysis by New York State Department of Agriculture & Markets.
ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lot (#700792) of product (zinc oxide) that they received, an investigation by…
Possible presence of glass fragments in CapriSun and Kool-Aid Jammers.
Simply Delicious is recalling Lemon Poppyseed bars because they were mispackaged with Coconut bars.
Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.
Presence of Particulate Matter: identified as dried skin.
Defective Delivery System: Defective stem valve causes leakage of the propellant in the spray canister delivering no drug or an inadequate amount of the drug to be delivered.
Lack of Assurance of Sterility: potential for leaking containers which lacks the assurance of sterility.
Marketed Without An Approved NDA/ANDA: Tainted product marketed as a dietary supplement. Product found to be tainted with sibutramine, an appetite suppressant that was withdrawn from the…
Failed impurities/degradation specifications: Out-of-specification result (for multiple batches) for an unknown impurity of Chlorhexidine gluconate.
Defective Delivery System; potential to have inaccurate dosage delivery
Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine, Phenolphthalein and/or Diclofenac.
Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.
Defective Delivery System; potential to have inaccurate dosage delivery
Presence of Particulate Matter: particulate matter identified as glass in one vial.
Failed impurities/degradation specifications: Out-of-specification result (for multiple batches) for an unknown impurity of Chlorhexidine gluconate.
Lack of Assurance of Sterility: Due to potential for leaking bags.
Failed impurities/degradation specifications: Out-of-specification result (for multiple batches) for an unknown impurity of Chlorhexidine gluconate.
Empirical Labs is recalling Liposomal Magnesium because of the potential for mold contamination.
The presence of a foreign material inside jugs of Bunge Vegetable Oil.
The presence of a foreign material inside jugs of Bunge Vegetable Oil.
The presence of a foreign material inside jugs of Bunge Vegetable Oil.
The presence of a foreign material inside jugs of Bunge Vegetable Oil.
The presence of a foreign material inside jugs of Bunge Vegetable Oil.
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.