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 Jul 18, 2018
Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCA Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Jul 18, 2018
Fluocinolone Acetonide Topical Solution, USP, 0.01%, 60 mL bottle, Rx Only, Manufactured by: Actavis Laboratories UT,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Jul 11, 2018
Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Icelandic Provisions Inc.
FDA (openFDA food enforcement)
Reported Jul 11, 2018
Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingenus Pharmaceuticals LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 4, 2018
fentanyl Citrate USP 5 mcg in 0.9% Sodium Chloride USP 0.5 mL, 10 mcg per mL prefilled syringe, Rx only, Advanced…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Pharma Inc.
FDA (openFDA drug enforcement)
Reported Jul 4, 2018
BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12/1/2018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Four Link Nutriworld
FDA (openFDA food enforcement)
Reported Jun 20, 2018
Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
FDA (openFDA device enforcement)
Reported Jun 20, 2018
Maxzide-25 (Triamterene and hydrochlorothiazide) tablets, USP, 37.5 mg/ 25 mg, 100-count bottle, Rx only, Mylan…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mylan Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Jun 20, 2018
HYDROmorphone HCl 0.5 mg per mL in 0.9% Sodium Chloride, 1 mL Total Volume in 3 mL syringe, Rx, PharMEDium Services,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PharMEDium Services, LLC
FDA (openFDA drug enforcement)
Reported Jun 13, 2018
NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
FDA (openFDA device enforcement)
Consumer productsReported Jun 12, 2018
Ashley Furniture Recalls Floor Lamps Due to Burn Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.dba Export India PVT Ltd.
CPSC
Reported May 30, 2018
Hot Dog Buns
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flowers Bakery Of Montgomery LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
T Shampoo For Hair and Body, Solution Coal Tar 3% (0.6% coal tar), 300 ml/10.1 fl. oz. bottles, Dermatologic Cosmetic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Milbar Laboratories, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 30, 2018
smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS II Knee System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Piperacillin and Tazobactam for Injection, USP 3.375 gram/vial* 10-count Single Use Vials per carton, Rx Only, Mfg. by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Apotex Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported May 23, 2018
Calendula Cream, calendula officinalis 1X HUS-10%, 2.5 oz. tubes, Distributed by Boiron Inc., Newtown Square, PA
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boiron Inc.
FDA (openFDA drug enforcement)
Reported May 16, 2018
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver-Visitec International Inc.
FDA (openFDA device enforcement)
Reported May 9, 2018
Docetaxel injection concentrate, 20 mg/mL, 1 mL vial, Rx only, Winthrop U.S. a business of Sanofi-Aventis U.S. LLC.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sanofi-Aventis U.S. LLC
FDA (openFDA drug enforcement)
Reported May 2, 2018
Fluocinolone Acetonide Topical Oil, 0.01% (Body Oil) 118.28 mL (4 fl. oz.) Rx Only, Manufactured by: Lyne Laboratories,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyne Laboratories, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported May 2, 2018
Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz (113g). No UPC.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Seabear Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Cystaran (cysteamine ophthalmic solution) 0.44%, 15 mL bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co. Inc.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leadiant Biosciences, Inc.
FDA (openFDA drug enforcement)
Reported Apr 25, 2018
Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lupin Pharmaceuticals Inc.
FDA (openFDA drug enforcement)
Reported Apr 25, 2018
Patient-Fitted Temporomandibular (TMJ) Right Mandibular Component part of TMJ Reconstruction Prosthesis System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TMJ Solutions Inc.
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.