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 May 20, 2026
Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only, Manufactured for: Endo USA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ENDO USA, Inc.
FDA (openFDA drug enforcement)
Reported May 20, 2026
Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oasis Medical, Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2026
NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acella Pharmaceuticals, LLC
FDA (openFDA drug enforcement)
Reported May 13, 2026
Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ajanta Pharma Ltd.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported May 13, 2026
Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B Braun Medical Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2026
Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breckenridge Pharmaceutical, Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2026
BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 213, LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 13, 2026
TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Central Admixture Pharmacy Services, Inc. (CAPS) Los Angeles
FDA (openFDA drug enforcement)
Reported May 13, 2026
DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 13, 2026
Enalapril Maleate Tablets, USP, 20 mg, 1,000-count bottle, Rx only, Manufactured by: Unique Pharmaceutical Laboratories…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JB Chemicals and Pharmaceuticals Ltd.
FDA (openFDA drug enforcement)
Reported May 13, 2026
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
FDA (openFDA drug enforcement)
Reported May 13, 2026
busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind,…
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 May 6, 2026
Systane, Lubricant Eye Gel, Night Gel, Sterile, 10g (0.35 oz), Processed in France for: Alcon Laboratiroes, Inc., Fort…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 6, 2026
Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.American Regent, Inc.
FDA (openFDA drug enforcement)
Reported May 6, 2026
Alendronate Sodium Oral Solution, 70 mg/75 mL, 75 mL, Rx only, 4 x 75 mL Single Dose Bottles, Distr. by: Hikma…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hikma Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported May 6, 2026
Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Scope Health
FDA (openFDA drug enforcement)
Reported May 6, 2026
iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed by: Thea Pharma…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thea Pharma, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 6, 2026
Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Water-Jel Technologies, LLC
FDA (openFDA drug enforcement)
Reported May 6, 2026
Phenylephrine Hydrochloride Injectable Solution, 40mg, 250*mL Bag, wells pharma of Houston, NDC 73702-122-03
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wells Pharma
6 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 29, 2026
Sterile Water for Injection USP, 3000 mL bags, Rx only, Pharmacy Bulk Package, B. Braun Medical Inc., Bethlehem, PA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 29, 2026
FRESHKOTE LUBRICANT EYEDROPS, Sterile, 0.33 FL OZ (10mL), Harrow Eye LLC, Nashville, TN USA.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harrow Eye LLC
FDA (openFDA drug enforcement)
Reported Apr 29, 2026
Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg, 1000-count bottle, Rx only, Manufactured for: Camber…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hetero Labs Limited (Unit V)
FDA (openFDA drug enforcement)
Reported Apr 29, 2026
Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leading Pharma, LLC
FDA (openFDA drug enforcement)
Reported Apr 29, 2026
Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles, Rx only, Manufacturer: Premier Medical Products, 1710…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Premier Dental Products Co.
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.