1,523 recalls · Class III, newest first
Reason Failed Stability Specification; product viscosity and or pH are below specification.
Reason Subpotent. drug
Reason Labeling: Incorrect or Missing Package Insert: the package insert for the potassium chloride 8 mEq and 10 mEq strength instead of the potassium…
Reason Failed Content Uniformity Specifications; at the 18 month time point.
Reason Failed Tablet/Capsule Specifications: Sandoz is recalling one lot of Hydroxychloroquine Sulfate Tablets, USP, 200mg, due to illegibility of the logo…
Reason Subpotent
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being carried out due to an incorrect expiration date assigned to a lot of…
Reason Discoloration; due to prolonged heat exposure.
Reason Failed Dissolution Specification:12 hour time point at 18 months of product shelf life.
Reason Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets.
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Defective Container: Stability samples of both products were noted to have some white solid product residue, identified as dried active ingredients…
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to be subpotent during the firm's routine testing.
Reason Subpotent; phenylephrine HCl
Reason Failed Tablet/Capsule Specifications: The products are being recalled due to chipped and broken tablets.
Reason Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the…
Reason Presence of Foreign Substance: This recall is being conducted due to the potential for extrinsic foreign particles in the API used to manufacture…
Reason Failed Dissolution Specifications: This recall is an extension of the recall initiated on 07/31/2013 for Bupropion HCl Extended-Release Tablets (XL)…
Reason Contraceptive tablets out of sequence: Contraceptive tablets out of sequence: Introvale (levonorgestrel and ethinyl estradiol tablets USP…
Reason Labeling: Incorrect or Missing Lot and/or Exp Date: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.