Independent register of U.S. FDA drug recalls · updated Oct 11, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class II · Moderate risk

methylPREDNIsolone ACETATE

Lack of Assurance of Sterility; autoclave parameters were not correct for one of two autoclaves used to sterilize the product.

Terminated Sterility / contamination RXQ Compounding LLC D-0012-2018
Class III · Low risk

Mobic (meloxicam)

Labeling: Incorrect or missing package insert. One lot of Mobic Tablets is packaged with an incorrect insert.

Terminated Labeling / mix-up Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0030-01 D-0007-2018
Class II · Moderate risk

Medline Skin Stapler RMVR

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Terminated Wrong potency / content Medline Industries Inc D-0314-2018
Class II · Moderate risk

Medline Anesthesia Kit

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Terminated Wrong potency / content Medline Industries Inc D-0306-2018
Class II · Moderate risk

Medline Hip Replacement

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Terminated Wrong potency / content Medline Industries Inc D-0304-2018
Class II · Moderate risk

Medline Debridement Tray

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Terminated Wrong potency / content Medline Industries Inc D-0300-2018
Class II · Moderate risk

Medline IV Start Kit

Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.

Terminated Wrong potency / content Medline Industries Inc D-0298-2018

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