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The Recall Registry is not a government service and does not issue recalls. We gather published recall notices from the U.S. Consumer Product Safety Commission, the U.S. Food and Drug Administration and the National Highway Traffic Safety Administration, and rewrite them in plain language. Always confirm the details with the issuing agency using the link on each recall page.

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Prescription medicine recalls

Prescription drugs recalled for contamination, potency or labelling.

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Highest riskSeriousWorth checkingLabelling issueTap any recall for the hazard and what to do

1,991 recalls · newest first

Food & drug recall · FDAFebruary 18, 2026Labelling issue

Cipla USA, Inc. — Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only

Prescription medicine · Cipla USA, Inc. · 164 cartons affected

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual…

Food & drug recall · FDAFebruary 17, 2026Serious

The Harvard Drug Group LLC — Midodrine Hydrochloride Tablets, USP, 5 mg, 50 Tablets (5 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6818-06.

Prescription medicine · The Harvard Drug Group LLC · 8892 cartons affected

Defective container; inadequately sealed blister packaging.

Food & drug recall · FDAFebruary 13, 2026Serious

Harbin Jixianglong Biotech Co., Ltd. — Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04; e) 100g, NDC 84385

Prescription medicine · Harbin Jixianglong Biotech Co., Ltd. · N/A affected

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before…

Food & drug recall · FDAFebruary 13, 2026Serious

AvKARE — Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only

Prescription medicine · AvKARE · N/A affected

Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.

Food & drug recall · FDAFebruary 13, 2026Serious

Harbin Jixianglong Biotech Co., Ltd. — Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04 Manufacturer: Harbin

Prescription medicine · Harbin Jixianglong Biotech Co., Ltd. · N/A affected

CGMP Deviations This recall has been initiated due to failing to complete process validation and bacterial endotoxin method validation before…

Food & drug recall · FDAFebruary 12, 2026Labelling issue

Slate Run Pharmaceuticals — Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only

Prescription medicine · Slate Run Pharmaceuticals · N/A affected

Labeling: Not Elsewhere Classified.

Food & drug recall · FDAFebruary 10, 2026Serious

LEO PHARMA INC — Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only

Prescription medicine · LEO PHARMA INC · 11,407 units affected

Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.

Food & drug recall · FDAFebruary 9, 2026Serious

Meitheal Pharmaceuticals, Inc — Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.

Prescription medicine · Meitheal Pharmaceuticals, Inc · 16,477 kits affected

Defective Delivery System: Missing or duplicated needles within the injection kit

Food & drug recall · FDAFebruary 5, 2026Serious