Complete FDA and NHTSA recall records dated in September 2017.
These records include useful source details for the selected month.
Ingredient used in the manufacture of these products was recalled due to a potential for Listeria monocytogenes contamination.
Crystallization: Particulate matter (Ketorolac Calcium Salt) was observed from several lots of retained samples.
Presence of Foreign Substance: customer complaint of blue foreign material identified as a portion of a nitrile glove was discovered in product.
Defective container: Oral solution leaking from container.
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.
