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

1,464 recalls · Class II, newest first

Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0199-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0198-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0197-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0196-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0195-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0194-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0193-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0192-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0191-2016
Class II · Moderate risk

Biest Td 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0190-2016
Class II · Moderate risk

Biest Td 67/33

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0189-2016
Class II · Moderate risk

Biest Td 50/50

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0188-2016
Class II · Moderate risk

Biest Td 50/50

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0187-2016
Class II · Moderate risk

Biest Cp 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0186-2016
Class II · Moderate risk

Biest Cp 80/20

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0185-2016
Class II · Moderate risk

Biest Cp 76/24: Dhea

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0184-2016
Class II · Moderate risk

Fomepizole Injection

Lack of Assurance of Sterility. A recent FDA inspection reported GMP violations potentially impacting product quality and sterility.

Terminated Sterility / contamination Navinta LLC NDC 0781-3182-73 D-0431-2015
Class II · Moderate risk

5% DEXTROSE Injection

Lack of Assurance of Sterility: there is a potential for solution to leak at the administrative port of the primary container.

Terminated Sterility / contamination Hospira Inc. NDC 0409-7100-02 D-0417-2015
Class II · Moderate risk

Haloperidol Oral Solution

Defective Container: Confirmed customer complaints of leaking bottles.

Terminated Packaging defect Safecor Health, LLC NDC 54838-0501-40 D-0661-2016

Recalls by year