US Drug Recall Register

FDA Drug Recalls

14,450 recalls · Class II, newest first

Class II · Moderate risk Terminated

Norepinephrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-002-01 D-0319-2022
Class II · Moderate risk Terminated

Morphine Sulfate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-427-01 D-0318-2022
Class II · Moderate risk Terminated

Fentanyl Citrate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-327-02 D-0317-2022
Class II · Moderate risk Terminated

Fentanyl Citrate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-327-01 D-0316-2022
Class II · Moderate risk Terminated

EPINEPHrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-027-01 D-0304-2022
Class II · Moderate risk Terminated

NOREPINEPHRINE 4 mg per 250 mL

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-451-01 D-0303-2022
Class II · Moderate risk Terminated

dilTIAZem HCl 125 mg per 125 mL

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-976-01 D-0302-2022
Class II · Moderate risk Terminated

Buprenorphine HCl

Reason Crystallization; identified as Buprenorphine free base

PAR Sterile Products LLC D-0087-2024
Class II · Moderate risk Terminated

Hand Sanitizer Foam

Reason Defective Container: Customer complaints for leaking bottles and dispensing issues.

Medline Industries Inc NDC 53329-970-12 D-0287-2022
Class II · Moderate risk Terminated

Flocinolone Acetonide 0.01% Topical Oil

Reason Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.

Amneal Pharmaceuticals of New York, LLC NDC 65162-703-86 D-0234-2022
Class II · Moderate risk Terminated

Flocinolone Acetonide 0.01% Topical Oil

Reason Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.

Amneal Pharmaceuticals of New York, LLC NDC 65162-704-86 D-0233-2022