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

2,357 recalls · Class II, newest first

Class II · Moderate risk

Norepinephrine Bitartrate in 5% Dextrose Injection

Incorrect product concentration on the overwrap label: The overwrap label incorrectly identified the product strength as 4 mg / 250 mL; however, the primary bag label correctly identified the product strength as 8 mg / 250 mL.

Ongoing Labeling / mix-up Baxter Healthcare Corporation D-0336-2024
Class II · Moderate risk

Vasostrict

Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Ongoing Wrong potency / content Par Sterile Products LLC D-0232-2024
Class II · Moderate risk

Medline Remedy Clinical TREAT Antifungal Cream

Labeling: Not Elsewhere Classified; Product labeling contains the claim of 'Paraben Free' while the product does in fact contain parabens as part of the formulation/ ingredient list.

Ongoing Labeling / mix-up MEDLINE INDUSTRIES, LP - Northfield D-0315-2024
Class II · Moderate risk

Premier Value Tussin Cough DM

CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.

Ongoing Microbial contamination Seaway Pharma Inc. D-0215-2024

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