1,523 recalls · Class III, newest first
Reason Labeling; labeled with incorrect EXP Date; Incorrect expiration date printed on the outer packaging. Package incorrectly states 5/2014 should…
Reason Impurities/Degradation Products: High Out of Specification results for a known impurity resulted at the 12-month room temperature time point.
Reason Impurities/Degradation Products: Out of specificiation results for impurities at the 18-month room temperature time point.
Reason Failed PH specification: The lots of Carboplatin Injection were manufactured from Carboplatin API lots which trended out of specification low pH.
Reason Adulterated Presence of Foreign Tablets/Capsules: Some bottles may contain a small number of Nexium 20 mg capsules intended for the Japanese market…
Reason Impurities/Degradation Products: Out of specification results for Related Compound during routine stability testing.
Reason Labeling: Label Mix-up: The product is being recalled because active ingredient in the Drug Facts box incorrectly states "Active Ingredients…
Reason CGMP Deviations: Shipment of product not approved for release.
Reason Labeling: Label Mix-up: The affected units were labeled incorrectly describing the product as "ointment" instead of "solution."
Reason Chemical Contamination: This product is being recalled because trace amounts of a plasticizer (Di-Octyl Phthalate) may be present in the product.
Reason Impurities/Degradation Products: High Out-of-specification results were obtained for both known and unknown impurities.
Reason Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store between 20¿ to 25¿C (68¿ to 77¿F)". Pitocin lot 225867 and part of…
Reason Impurities/Degradation Products: A confirmed out of specification result for Leukine sargramostin lot B18827 occurred at the three month time point.
Reason Subpotent (Multiple Ingredient) Drug: Low out of specification assay results for the hydrocodone bitartrate ingredient was found.
Reason Defective Container; damaged blister units
Reason Impurities/Degradation Products: The product was found to contain a slightly out of specification level of bromides, exceeding the bromides limit for…
Reason Subpotent; fluocinolone acetonide
Reason Subpotent; fluocinolone acetonide
Reason Adulterated Presence of Foreign Tablets: Customer complaint that some Endocet 10 mg/325 mg tablets were found mixed in a bottle with Endocet 10…
Reason Subpotent Drug: Salicylic acid is subpotent.
Reason Subpotent Drug: Salicylic acid is subpotent.
Reason Subpotent Drug: Salicylic acid is subpotent.
Reason Subpotent Drug: Salicylic acid is subpotent.
Reason Subpotent Drug: Salicylic acid is subpotent.
Reason Labeling: Label Mix-up: This recall was initiated after identifying that the label statement on the blister strip regarding the maximum number of…