Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the…
Potential foreign material (wood-like material)
undeclared allergen ingredient (wheat) on product label for flour Gorditas.
Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)
Label declares tofu but it does not declare soy.
Potential contamination with foreign material (plastic)
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Undeclared allergens: Soy lecithin
Undeclared allergen (milk).
Potential foreign material (wood-like material)
Recall was initiated due to potential failure of the seal and potential to be contaminated with Clostridium botulinum.
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Potential foreign material (wood-like material)
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
Turkey BLT on Sourdough Sandwiches being recalled due to the product having the incorrect sandwich (Peanut Butter & Jelly) in the clamshell container. This incorrect product in the…
Various non-shelf stable packaged vegetables missing "Keep Refrigerated" statement on label.
CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit.
CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
Sub-Potent Drug: The stability batch showed a subpotent result, which does not meet the product specifications of 90.0-110.0% of the label claim.
Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.
Browse recent months with enough recall history for useful comparison.
