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 Apr 17, 2024
Isotretinoin Capsules, USP 40mg, 30-count 3x10 blister packs per carton, Rx Only, Manufactured For: Teva…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
FDA (openFDA drug enforcement)
Reported Apr 17, 2024
Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coastal Companies dba Hearn Kirkwood
FDA (openFDA food enforcement)
Reported Apr 10, 2024
HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.O&m Halyard, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2024
HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Puritan Medical Products Company, LLC
FDA (openFDA device enforcement)
Reported Mar 27, 2024
Medtronic DLP Vessel Cannula, Model Number REF 30000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains 40mg of omeprazole and 1,680mg…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch Health Companies, Inc.
FDA (openFDA drug enforcement)
Reported Mar 6, 2024
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
FDA (openFDA device enforcement)
Reported Feb 28, 2024
GORE VIABIL Short Wire Biliary Endoprosthesis, Product labeled as (1) Catalog Number VSWVH1008, 10 mm x 8 cm; with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W.L. Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Feb 7, 2024
FentaNYL citrate PF, 1000 mcg per 100 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3355, for IV use only; Leiters…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Denver Solutions, LLC dba Leiters Health
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 31, 2024
Benzonatate Capsules, USP, 100 mg, 100 Capsules (10 capsules x 10 unit dose cards), Rx only, Distributed by: American…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amerisource Health Services LLC
FDA (openFDA drug enforcement)
Reported Jan 31, 2024
Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IntegraDose Compounding Services LLC
FDA (openFDA drug enforcement)
Reported Jan 31, 2024
Achieva 1.5T, Model No. 781178, 781196, 781296
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Philips North America
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2024
Azurity Pharmaceuticals, Inc. recalls Zendedi dextroamphetamine sulfate tablets, 30 mg due to Mislabeled package
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Azurity Pharmaceuticals, Inc.
FDA (recalls & safety alerts)
Reported Jan 24, 2024
Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Par Sterile Products LLC
FDA (openFDA drug enforcement)
Reported Jan 24, 2024
Link Patella Glide Resection Guide- For the implantation of the Endo-Model Knee System as part of a total knee…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Waldemar Link GmbH & Co. KG (Mfg Site)
FDA (openFDA device enforcement)
Reported Jan 17, 2024
Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vita 360, LLC
FDA (openFDA food enforcement)
Reported Jan 10, 2024
Reverse Shoulder System e+, REF 509-01-032, RSP Humeral Socket Insert, Sz. 32mm, Semi-Constrained, Sterile H2o2, CE 2797
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2024
Leiters Health recalls Leiters, Compounding Health Vancomycin IV Bags, Phenylephrine IV Bags, and Fentanyl IV Bags due to Potential for superpotent drug
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Leiters Health
FDA (recalls & safety alerts)
Reported Dec 27, 2023
ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Nov 8, 2023
Opium Tincture, USP (Deodorized), 10 mg/mL of anhydrous morphine, packaged in 118 mL (4 Fl oz) bottles, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Edenbridge Pharmaceuticals, LLC
FDA (openFDA drug enforcement)
Reported Oct 25, 2023
MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution Drops 1% - 0.5% - 2.5%…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Imprimis NJOF, LLC
FDA (openFDA drug enforcement)
Reported Oct 18, 2023
Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g), plastic package (i.e.) Clamp shell, 8 package per case,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairfield Gourmet Food Corp. d/b/a David's Cookies
FDA (openFDA food enforcement)
Reported Oct 11, 2023
Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Imprimis NJOF, LLC
FDA (openFDA drug enforcement)
Reported Oct 4, 2023
Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%), packaged in 90-count plastic jar, further packaged in…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.RB Health (US) LLC
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.