US Drug Recall Register

FDA Drug Recalls

2,661 recalls, newest first

Class II · Moderate risk Ongoing

Motrin Ib Caplets 24ct Sku999394

Reason CGMP Deviations: product held outside appropriate storage temperature conditions.

Family Dollar Stores, Llc. D-1373-2022
Class II · Moderate risk Ongoing

AMBI Skincare Fade Cream Normal Skin

Reason cGMP deviations: product stored outside of labeled temperature requirements.

Family Dollar Stores, Llc. D-0976-2022
Class II · Moderate risk Ongoing

Alcohol Antiseptic 80%

Reason CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

A.P. Nonweiler D-1142-2022
Class II · Moderate risk Ongoing

Premium Nature Instant Hand Sanitizer

Reason Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.

AMS Packaging Inc D-1148-2022
Class II · Moderate risk Ongoing

Daytrana

Reason Defective Delivery System: customer complaints exceeded respective action limits.

Noven Pharmaceuticals Inc NDC 68968-5552-3 D-0889-2022
Class II · Moderate risk Ongoing

Erythromycin Topical Gel USP

Reason CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

McKesson Corporation dba McKesson Drug Company NDC 63739-053-68 D-0851-2022
Class II · Moderate risk Ongoing

Betamethasone Dipropionate Ointment USP

Reason CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

McKesson Corporation dba McKesson Drug Company NDC 63739-996-65 D-0850-2022
Class II · Moderate risk Ongoing

Lidocaine Prilocaine Cream USP

Reason CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

McKesson Corporation dba McKesson Drug Company NDC 63739-054-66 D-0849-2022
Class II · Moderate risk Ongoing

Lidocaine Hydrochloride Topical Solution USP 4%

Reason CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.

McKesson Corporation dba McKesson Drug Company NDC 63739-977-64 D-0848-2022