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 Oct 25, 2019
Taylor’s Sausage Inc. Recalls Ready-To-Eat Meat and Poultry Products Due to Mislabeling
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor's Sausage, Inc.
USDA FSIS
Reported Oct 23, 2019
Dextroamphetamine Sacharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets, Mixed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aurobindo Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Oct 23, 2019
Dunkin' Mocha Swirl Prepared Exclusively for Dunkin' Brands Canton, MA 02021 Net Contents 64 FL OZ/1.89L Not For Resale
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lyons Magnus, Inc.
FDA (openFDA food enforcement)
Reported Oct 23, 2019
Pioglitazone Hydrochloride Tablets USP 15 mg, 30 count bottles, Rx only, Manufactured for: Macleods Pharma USA, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Macleods Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Oct 16, 2019
Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2019
20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product # RMS22606 - Product Usage: RMS HlgH-Flo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Repro-Med Systems, Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Stryker Neurovascular, Merci 9F, 80cm, Balloon Guide Catheter, REF 90077, CE 0459, UPN Product No. 90077, UDI #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Oct 9, 2019
Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer GmbH
FDA (openFDA device enforcement)
Reported Oct 2, 2019
Silk Soymilk Vanilla Bag-In-Box. One, 2.5 gallon bag per box. 2.5 gal Bag-In-Box to be used in a dispensing machine at…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Danone
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Savory Tuna salad 16 oz. packaged in Clear PP containers UPC 4122033749
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bakkavor USA
FDA (openFDA food enforcement)
Reported Sep 18, 2019
Pramipexole Dihydrochloride Tablets 0.125 mg,90-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Macleods Pharma USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 28, 2019
Luer Lock Set - Catalog # MPC-125, for IV administration sets.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Molded Products Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2019
SunTech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suntech Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2019
Lidar System for Erosion Flume Application Class 1 Laser Product Product Usage: Product is installed and fixed above a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Astra, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2019
PTS Panels Lipid Panel test strip: IVD Lipid Panel Test Strips Ref Number: 1710 Product Usage: PTS Panels Lipid Panel…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Polymer Technology Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops, packaged in 5mL bottles, Rx only, ImprimisRX NJ 1705 Route 46…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ImprimisRx NJ
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 31, 2019
MONSEL'S (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dercher Enterprises, Inc., dba Gordon Laboratories
FDA (openFDA drug enforcement)
Reported Jul 31, 2019
Versa - Kath Mini Kit, with plastic L.O.R Syringe 12g X 12in (30.5 cm), 5 units, Sterile ED, REF 181-2112, RX, (01)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epimed International, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 31, 2019
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FoodScience Corporation
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension, (equivalent to 10 mg hydrocodone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tris Pharma Inc.
FDA (openFDA drug enforcement)
Reported Jul 19, 2019
Bayer recalls Kogenate® Kogenate® FS antihemophilic factor (recombinant) due to Mislabeling-contains the FVIII hemophilia A treatment, Jivi® antihemophilic…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Bayer
FDA (recalls & safety alerts)
Reported Jul 17, 2019
Soy Sauce, 10 FL OZ
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baumer Foods Inc.
FDA (openFDA food enforcement)
Reported Jul 10, 2019
Esterified Estrogens & Methyltestosterone Tablets, USP 0.625 mg/1.25 mg, 100-count bottles, Rx Only, Manufactured by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amneal Pharmaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 3, 2019
Mosaic 310 Bioprosthesis, Mitral, REF 310C29 - Product Usage: Replacement of malfunctioning native or prosthetic aortic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
4 more products in this recall
FDA (openFDA device 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.