How do I check if my Medicine & Drugs product is recalled?

Find your product or brand in the live list below, or search it directly on EveryRecall. Recalls target specific lot numbers and date codes, so match the affected lots in the official notice against your own product.

What does a Class I recall mean?

Class I is the most serious recall class — a reasonable probability that using the product will cause serious harm or death. Class II means temporary or reversible harm is possible; Class III means harm is unlikely.

Medication & drug recalls (2026)

Live prescription and over-the-counter drug recalls from the FDA enforcement database and Health Canada.

Live data · updated continuously · newest record August 12, 2026 · 40 recent recalls shown.

Popular medicine & drugs brands

Is Tylenol recalled? Is Advil recalled? Is Zantac recalled?

Recent medicine & drugs recalls

Lactated Ringer's Injection USP, 1000 mL EXCEL container, Rx only, L7500, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-00Class I Aug 12, 2026

FDA drug enforcement · USB BRAUN MEDICAL INC

Presence of Particulate matter.
View official record →
Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois, 60047, NDC…Class I Aug 10, 2026

FDA drug enforcement · USFresenius Kabi USA, LLC

Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
View official record →
Acthar Gel (repository corticotropin injection), 5 mL multiple-dose vial, Rx Only, Mfd. for: Mallinckrodt ARD LLC, Bridgewater, NJ 08807, NDC 63004-8710-1 & ND…Class II Aug 6, 2026

FDA drug enforcement · USMallinckrodt Hospital Products Inc.

Presence of particulate matter: glass and stopper piece
View official record →
Morphine Sulfate Injection, USP, 2 mg /mL, 1 mL single-dose Simplist prefilled syringes, For Intramuscular or Intravenous use, Rx only, Fresenius Kabi, Lake Zu…Class I Aug 4, 2026

FDA drug enforcement · USFresenius Kabi USA, LLC

Labeling: Label Mixup: MicroVault labeled as Morphine 2 mg/1 mL, contains a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL.
View official record →
Optiray Imaging Bulk Package-350, Ioversol Injection 74%, 350 mg/mL Organically Bound Iodine, 500 mL Multiple-Dose Vial, Rx only, Sterile Solution, Manufacture…Class I Jul 31, 2026

FDA drug enforcement · USLiebel-Flarsheim Company LLC

Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.
View official record →
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SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste…Class II Jul 29, 2026

FDA drug enforcement · USApollo Care, LLC

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
View official record →
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202…Class II Jul 29, 2026

FDA drug enforcement · USApollo Care, LLC

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
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PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distrib…Class II Jul 29, 2026

FDA drug enforcement · USShilpa Medicare Limited

Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
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SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65…Class II Jul 29, 2026

FDA drug enforcement · USApollo Care, LLC

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
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SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste…Class II Jul 29, 2026

FDA drug enforcement · USApollo Care, LLC

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
View official record →
Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, …Class II Jun 24, 2026

FDA drug enforcement · USQuVa Pharma, Inc.

Failed Impurities/Degradation Specifications
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Carton Label: MAJOR, Methylergonovine Maleate Tablets, USP, 0.2 mg, 20 TABLETS (2 x 10), Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapo…Class II Jun 16, 2026

FDA drug enforcement · USThe Harvard Drug Group LLC

Subpotent Drug
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Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle, Rx only, Manufactured by: Inventia Healthcare Limited, Additional Ambernath, M.I.D.C., Amb…Class II Jun 5, 2026

FDA drug enforcement · USInventia Healthcare Limited

Failed Dissolution Specifications
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Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Th…Class II Jun 4, 2026

FDA drug enforcement · USAmgen, Inc.

Presence of Foreign Substance.
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Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spa…Class II Jun 4, 2026

FDA drug enforcement · USBreckenridge Pharmaceutical, Inc.

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
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Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g), P…Class II Jun 2, 2026

FDA drug enforcement · USDabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection
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Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g) tubes, P…Class II Jun 2, 2026

FDA drug enforcement · USDabur India Limited

CGMP Deviations; deficiencies observed during FDA inspection
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DISCOUNT drug mart, EXTRA STRENGTH, ANTACID TABLETS, Calcium Carbonate 750 mg, 96 Tablets, Distributed by: Drug Mart- Food Fair Medina, OH 44256, UPC: 0 93351 …Class II May 28, 2026

FDA drug enforcement · USGuardian Drug Co. Inc.

Presence of foreign substance: small metallic particles in chewable tablets.
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KIRKLAND Signature, ULTRA STRENGTH ANTACID, Calcium Carbonate, 1000 mg, 265-count bottle, MANUFACTURED BY: GUARDIAN DRUG COMPANY, INC., 2 CHARLES COURT/DAYTON,…Class II May 28, 2026

FDA drug enforcement · USGuardian Drug Co. Inc.

Presence of foreign substance: small metallic particles in chewable tablets.
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Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) 100-count carton, NDC 0555-1054-56, with 10x10 blister packs NDC 0555-1054-60; b) 30-count carton, …Class II Apr 6, 2026

FDA drug enforcement · USTeva Pharmaceuticals USA, Inc

Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
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Discount Drug Mart Food Market, Cough Drops, Menthol -Cough Suppressant Anesthetic, 30-count bag, Distributed By: Drug Mart-Food Fair, Medina, Ohio 44256, Made…Class II Mar 20, 2026

FDA drug enforcement · USXiamen Kang Zhongyuan Biotechnology Co., Ltd.

This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
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Discount Drug Mart Food Market, Cough Drops, Menthol- Cough Suppressant Anesthetic, Honey Lemon, 30-count bag, Distributed By: Drug Mart-Food Fair, Medina, Ohi…Class II Mar 20, 2026

FDA drug enforcement · USXiamen Kang Zhongyuan Biotechnology Co., Ltd.

This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
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Product label: Temozolomide Capsules, 5mg, packaged in 5-capsule bottles, Rx only, Manufactured for: Rising Pharmaceuticals, Inc., Allendale, NJ 07401, Country…Class II Mar 3, 2026

FDA drug enforcement · USRising Pharma Holding, Inc.

Failed Impurities/Degradation Specifications: An out-of-specification result observed during 9th-month long term stability testing
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Sterile Eye Drops ORIGINAL FORMULA (tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15mL) bottles; a) Good Sense Sterile Eye Drops, Distributed By: Perrigo Direct, Inc…Class II Mar 3, 2026

FDA drug enforcement · USK.C. Pharmaceuticals, Inc

Lack of Assurance of Sterility
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Dry Eye Relief Eye Drops, (glycerin 0.2%, hypromellose 0.2% and polyethylene glycol 400 1%) 0.5 FL OZ (15 mL) bottles; a) GERI CARE, Distributed by: Gericare …Class II Mar 3, 2026

FDA drug enforcement · USK.C. Pharmaceuticals, Inc

Lack of Assurance of Sterility
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Sterile EYE DROPS REDNESS LUBRICANT (glycerin 0.25% and naphazoline HCl 0.012%), 0.5 fl oz (15 mL) bottles; a) Industrial Eye Relief, Distributed by: Cintas Co…Class II Mar 3, 2026

FDA drug enforcement · USK.C. Pharmaceuticals, Inc

Lack of Assurance of Sterility
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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 Isotop…Class III Feb 19, 2026

FDA drug enforcement · USRadnostix

Failed Tablet/Capsule Specifications
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Nilotinib Capsules, 150 mg per capsule, packaged in cartons, Rx only, Manufactured by: Cipla Ltd., Verna, Goa, India, Manufactured for: Cipla USA, Inc., 10 Ind…Class III Feb 18, 2026

FDA drug enforcement · USCipla USA, Inc.

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
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Nilotinib Capsules, 200 mg per capsule, packaged in cartons, Rx only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059…Class III Feb 18, 2026

FDA drug enforcement · USCipla USA, Inc.

Failed Tablet/Capsule Specifications: Observed OOS results at 6-months long-term stability condition for Description test and Appearance by Visual Inspection test.
View official record →
Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet pac…Class II Dec 26, 2025

FDA drug enforcement · USGOLD STAR DISTRIBUTION INC

CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
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MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distributed by mR. 7Class I Dec 15, 2025

FDA drug enforcement · USStuffbyNainax

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
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Duloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactured by: Towa Pharmaceuticals Europe, S.L. Marotrelles, (Barcelona), Sp…Class II Nov 24, 2025

FDA drug enforcement · USBreckenridge Pharmaceutical, Inc.

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
View official record →
Duloxetine Delayed-Release Capsules, USP, 60 mg, 1000-Capsule bottles, Rx Only, Manufactured by: Towa Pharmaceuticals Europe, S.L. Marotrelles, (Barcelona), Sp…Class II Nov 24, 2025

FDA drug enforcement · USBreckenridge Pharmaceutical, Inc.

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
View official record →
Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0Class I Oct 8, 2025

FDA drug enforcement · USMohamed Hagar

Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
View official record →
chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 (10x10) blisterpacks, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. 50 Tablet…Class II Aug 27, 2025

FDA drug enforcement · USAmerisource Health Services LLC

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was …
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Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02Class II Apr 15, 2025

FDA drug enforcement · USPharmadel, LLC

cGMP deviations
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Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99Class II Apr 15, 2025

FDA drug enforcement · USPharmadel, LLC

cGMP deviations
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PRASUGREL TABLETS, 5 mg, 30 tablet bottles, Rx only, packaged by GSMS, Incorporated, Camarillo, CA 93012 NDC 51407-444-30Class II Mar 5, 2025

FDA drug enforcement · USGolden State Medical Supply Inc.

Failed Dissolution Specifications
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Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc.…Class II Jan 24, 2025

FDA drug enforcement · USRemedyRepack Inc.

CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit.
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Clonazepam Orally Disintegrating Tablet, USP, 2 mg, C-IV, Rx Only, 60 Tablets per carton, 10 blister cards containing 6 tablets each, Distributed by: PAR Pharm…Class I Nov 18, 2024

FDA drug enforcement · USEndo USA, Inc.

Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength.
View official record →

What to do if your medicine & drugs is recalled

Match the lot. Recalls target specific lot numbers, date codes, or UPCs — not whole brands. Find the affected codes in the official notice and compare them to your product.
Check the class. Class I is most serious (risk of serious harm); Class II is temporary/reversible; Class III is low-risk labeling issues.
Don't use it if it matches. Stop using the product, and follow the notice's instructions — usually return for a refund or safe disposal.
Re-check periodically. Recalls are announced constantly. This page and our RSS feed update continuously.

Important. A listing here doesn't mean every product from that brand is affected, and an empty list isn't a safety guarantee. Always confirm your exact product against the linked official notice. EveryRecall is independent and not affiliated with any government agency.