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.
972 stored notices, reported between Jun 20, 2012 and Sep 23, 2026. Newest first.
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)
Reported Aug 14, 2024
Lunds & Byerlys grilled chicken caesar salad, Net Wt: 9.0 oz. (255.2g) UPC 0 18169-66428 5. Lunds & Byerlys, Edina, MN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lunds Mitchell Rd LLC
FDA (openFDA food enforcement)
Reported Aug 7, 2024
SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2024
Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Global Widget LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 24, 2024
Aurobindo Pharma USA, Inc. recalls Healthy Living Migraine Relief Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg tablets due to Device & Drug…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Aurobindo Pharma USA, Inc.
FDA (recalls & safety alerts)
Reported Jul 24, 2024
UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in partial hip arthroplasty. Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2024
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Jul 17, 2024
Endo USA, Inc recalls Par Pharmaceutical Clonazepam Orally Disintegrating Tablets, USP (C-IV) 0.25 mg tablets due to Mislabeled with the incorrect strength on…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Endo USA, Inc.
FDA (recalls & safety alerts)
Reported Jul 17, 2024
Non-sterile, single use, disposable gloves intended for medical purposes to be worn on the hands of examiners to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Svs LLC
FDA (openFDA device enforcement)
Reported Jul 17, 2024
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tailstorm Health Inc.
FDA (openFDA drug enforcement)
Reported Jul 10, 2024
Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only, Manufactured for: Accord…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Accord Healthcare, 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.