Labeling and dosing error recalls
Nothing is contaminated in these recalls — the package says the wrong thing. That can mean a bottle holding a different strength than the label states, two products packed in the wrong carton, or missing directions. For medication these can matter as much as contamination, because the dose taken is the wrong one.
982 stored notices, reported between Jun 20, 2012 and Nov 11, 2026. Newest first.
Reported Feb 26, 2025
Wegmans, Organic Almonds Dry Roasted Salted, 12oz clear bag, 12 bags per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United Natural Trading Inc. dba Woodstock Farms
FDA (openFDA food enforcement)
Reported Feb 12, 2025
Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with a clear plastic lid with a white label,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dierbergs Markets, Inc.
FDA (openFDA food enforcement)
Reported Feb 12, 2025
Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oxoid Limited
FDA (openFDA device enforcement)
Reported Feb 12, 2025
Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PAI Holdings, LLC. dba Pharmaceutical Associates Inc.
FDA (openFDA drug enforcement)
Reported Jan 29, 2025
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Renal Soultions USA, Corporation
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mylan Institutional, Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 18, 2024
Nestle Health Services Nutren 2.0 kCal/mL, Calorically Dense Complete Nutrition with Fiber Unflavored. 1000mL (1.1QT).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle Health Science
FDA (openFDA food enforcement)
Reported Dec 18, 2024
Levothyroxine Sodium Tablets USP, 125 mcg, packaged in a) 90-count bottles (NDC 0378-1813-77) and b) 1000-count bottles…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Viatris Inc.
10 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 11, 2024
Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accord Healthcare, Inc.
FDA (openFDA drug enforcement)
Reported Dec 4, 2024
AMS Artificial Urinary Sphincter Control Pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2024
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Nov 27, 2024
NovoHip Biolox Ball Head 32mmL Ref: 1345-2803 NovoHip Total Hip System - NovoHip Total Hip System is a non-cemented hip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novosource, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2024
Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Padagis US LLC
FDA (openFDA drug enforcement)
Reported Nov 20, 2024
Perio Maintenance Rinse 0.63% Stannous Fluoride Concentrated Solution, Rx Only, Net Wt. 10 oz. (283.5 g) pumps, Mint…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Industries
FDA (openFDA drug enforcement)
Reported Nov 19, 2024
Endo, Inc. recalls Par Pharmaceutical Clonazepam Orally Disintegrating Tablets, USP (C-IV) due to Mislabeled with the incorrect strength on the carton
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Endo, Inc.
FDA (recalls & safety alerts)
Reported Nov 6, 2024
Chlorpheniramine Maleate 4 mg tablets, 24-count bottle, Manufactured For: Athlete's Needs, Novi, MI 48377, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BLI International, Inc.
FDA (openFDA drug enforcement)
Reported Oct 16, 2024
Minute Maid Zero Sugar Lemonade 12 cans carton UPC 0 25000 12115 9 CANNED UNDER THE AUTHORITY OF THE COCA-COLA COMPANY,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.COCA COLA Consolidated LLC
FDA (openFDA food enforcement)
Reported Oct 16, 2024
Inspire Model 4340 Respiratory Sensing Lead, component of the Inspire Upper Airway Stimulation (UAS) system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inspire Medical Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Mupirocin Ointment, USP, 2%, 22 g, Rx only, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Sep 18, 2024
Biolox Option Taper Sleeve, Type 1 Taper, Standard Neck - Indicated for use in total hip replacement with cemented or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2024
Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Sep 4, 2024
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neurovision Medical Products Inc.
FDA (openFDA device enforcement)
Reported Aug 28, 2024
Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
FDA (openFDA drug enforcement)
Free recall alerts
Get alerted about new Labeling and dosing errors recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Related categories
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.