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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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2,102 recalls · newest first

Food & drug recall · FDAFebruary 26, 2026Serious

New Life Pharma LLC — Semaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.

Prescription medicine · New Life Pharma LLC · 820 vials affected

Lack of Assurance of Sterility

Food & drug recall · FDAFebruary 26, 2026Serious

New Life Pharma LLC — Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-06

Prescription medicine · New Life Pharma LLC · 2 vials affected

Lack of Assurance of Sterility

Food & drug recall · FDAFebruary 26, 2026Serious

New Life Pharma LLC — Tirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-03.

Prescription medicine · New Life Pharma LLC · 23 vials affected

Lack of Assurance of Sterility

Food & drug recall · FDAFebruary 26, 2026Serious

MACLEODS PHARMA USA, INC — Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, Rx Only

Prescription medicine · MACLEODS PHARMA USA, INC · 1315 bottles affected

Subpotent Drug

Food & drug recall · FDAFebruary 26, 2026Serious

New Life Pharma LLC — Tirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-04.

Prescription medicine · New Life Pharma LLC · 45 vials affected

Lack of Assurance of Sterility

Food & drug recall · FDAFebruary 24, 2026Serious

MYLAN PHARMACEUTICALS INC — Amnesteem (Isotretinoin) Capsules, USP 40 mg, packaged in 3 x 10-Count Prescription Packs, Rx Only

Prescription medicine · MYLAN PHARMACEUTICALS INC · 34850 blister packs affected

Failed Dissolution Specifications

Food & drug recall · FDAFebruary 19, 2026Labelling issue

Radnostix — Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 6920

Prescription medicine · Radnostix · 2,699 blister cartons affected

Failed Tablet/Capsule Specifications

Food & drug recall · FDAFebruary 18, 2026Serious

HTO Nevada Inc. dba Kirkman — MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles

Prescription medicine · HTO Nevada Inc. dba Kirkman · 178 bottles affected

Stability Data Does Not Support Expiry Date.

Food & drug recall · FDAFebruary 18, 2026Labelling issue

Cipla USA, Inc. — Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only

Prescription medicine · Cipla USA, Inc. · 271 cartons - Ex: 84 outer cartons x 4 inner cartons x 4 blisters x 7 capsules 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 18, 2026Serious

HTO Nevada Inc. dba Kirkman — MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles

Prescription medicine · HTO Nevada Inc. dba Kirkman · 243 bottles affected

Stability Data Does Not Support Expiry Date.

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 18, 2026Serious

HTO Nevada Inc. dba Kirkman — FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles

Prescription medicine · HTO Nevada Inc. dba Kirkman · 27,380 bottles. affected

Stability Data Does Not Support Expiry Date.

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

Fresenius Kabi Compounding, LLC — ketamine HCl, 1,000 mg, 1,000 mg per 100 mL (10 mg per mL) in Sodium Chloride Injection, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-050-56

Prescription medicine · Fresenius Kabi Compounding, LLC · 1410 bags affected

Lack of Assurance of Sterility

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