Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class II · Moderate risk

Sterile Cannabidiol

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Terminated Sterility / contamination BIOTA Biosciences LLC D-1329-2020
Class II · Moderate risk

Sterile Cannabidiol

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Terminated Sterility / contamination BIOTA Biosciences LLC D-1328-2020
Class II · Moderate risk

Sterile Curcumin

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Terminated Sterility / contamination BIOTA Biosciences LLC D-1327-2020
Class II · Moderate risk

Sterile Cannabidiol

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Terminated Sterility / contamination BIOTA Biosciences LLC D-1326-2020
Class II · Moderate risk

Aloprim (allopurinol sodium)

Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.

Terminated Failed specification Mylan Institutional LLC D-1271-2020
Class II · Moderate risk

Infuvite PEDiatric Pharmacy

Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins

Terminated Packaging defect Sandoz, Inc NDC 54643-5647-0 D-1259-2020
Class II · Moderate risk

Lisinopril Tablets USP

Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril tablets inside of 2 sealed bottles of 20 mg/1000 count bottles.

Terminated Labeling / mix-up Lupin Pharmaceuticals Inc. NDC 68180-0981-03 D-1250-2020
Class II · Moderate risk

Nizatidine Oral Solution

CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.

Terminated Nitrosamine impurity Amneal Pharmaceuticals of New York, LLC NDC 60846-301-15 D-1253-2020
Class II · Moderate risk

Estradiol

cGMP deviations: Presence of foreign material (Teflon)introduced at the production level.

Terminated Particulate / foreign matter B & B Pharmaceuticals, Inc. NDC 63275-9900-8 D-1244-2020

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