Prescription and over-the-counter medication recalls
Drug recalls come from the FDA's drug enforcement reports. They range from a wrong label to a product that could be harmful, and the risk level on each notice is the FDA's own classification. Never stop a prescribed medication on the strength of a recall notice alone — the notice will say whether to return it, and your prescriber or pharmacist decides what replaces it.
4,474 stored notices, reported between Jun 20, 2012 and Sep 9, 2026. Newest first.
Reported Jun 17, 2020
Lisinopril Tablets, USP, 5 mg, Rx Only, 1000-count bottle, Manufactured for: Lupin Pharmaceuticals Inc., Baltimore, MD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jun 17, 2020
Unasyn (ampicillin sodium/sulbacatam) for injection, 1.5 g* per vial, Rx Only, 10 vials/carton, Made in Italy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer Inc.
FDA (openFDA drug enforcement)
Reported Jun 17, 2020
oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.QuVa Pharma, Inc.
FDA (openFDA drug enforcement)
Reported Jun 17, 2020
Clonidine Hydrochloride Tablets, USP 0.1 mg 100-count bottles, Rx only, Manufactured by: Unichem Laboratories LTD.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Unichem Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
NP Thyroid 30, Thyroid Tablets, USP, 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured For: Acella…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Acella Pharmaceuticals, LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
Lamotrigine Tablets, USP, 150 mg, Rx Only, a) 60 count Bottle, NDC 42291-368-60, b) 500 count Bottle, NDC 42291-368-50,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.AVKARE Inc.
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets ( Mixed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
Doxycycline Hyclate Tablets, USP, 100 mg, packaged in a) 3x10 unit dose cartons (NDC 0904-0430-04) and b) 5 x 10 unit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Harvard Drug Group
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
Carbamazepine Tablets, USP 200 mg, packaged in a 500-count bottle, Rx only, Manufactured by: Torrent Pharmaceuticals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torrent Pharma Inc.
FDA (openFDA drug enforcement)
Reported Jun 10, 2020
Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Triova Pharmaceuticals LLC
FDA (openFDA drug enforcement)
Reported Jun 3, 2020
Lamotrigine Tablets, USP, 150 mg, 20,000-count bulk container, Manufactured by: Jubilant Cadista Pharmaceuticals Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Jubilant Cadista Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 3, 2020
Doxycycline Hyclate tablets USP, 100 mg, packaged in bottles a) 6-count (NDC 55289-866-06), b) 10-count (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PD-Rx Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Jun 3, 2020
Doxycycline Hyclate Tablets USP, 100 mg, packaged in a) 50-count bottle (NDC 0143-2112-50), b) 500-count bottle (NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.West-Ward Columbus Inc.
FDA (openFDA drug enforcement)
Reported Jun 3, 2020
LidoPatch (lidocaine HCl 3.6%, menthol 1.25%) Pain Relief Patch, packaged in 1 patch/box (NDC 10882-527-01); 30…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wuhan Bingbing Pharmaceutical Co., Ltd.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported May 27, 2020
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ICU Medical Inc.
FDA (openFDA drug enforcement)
Reported May 27, 2020
Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.InvaGen Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported May 27, 2020
Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only, Manufactured for: Mylan Institutional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Institutional LLC
FDA (openFDA drug enforcement)
Reported May 27, 2020
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.West-Ward Columbus Inc.
FDA (openFDA drug enforcement)
Reported May 20, 2020
ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Glaxosmithkline Consumer Healthcare Holdings
2 more products in this recall
FDA (openFDA drug enforcement)
Reported May 20, 2020
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MasterPharm LLC
FDA (openFDA drug enforcement)
Reported May 20, 2020
Memantine Hydrochloride Extended-Release Capsules, 28 mg, 100 capsules per unit dose cartons, Rx only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.The Harvard Drug Group
FDA (openFDA drug enforcement)
Reported May 13, 2020
Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz, Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2020
Epinephrine Injection USP, 0.3 mg (Auto-Injector), 0.3 mg/ 0.3 mL pre-filled syringe, Rx Only, Manufactured for Teva…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported May 6, 2020
Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL) USP 480 mL bottles, Rx Only Distributed by: Gemini Laboratories, LLC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amneal Pharmaceuticals
FDA (openFDA drug enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.