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 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)
Reported Oct 4, 2023
Eligard (leuprolide acetate) for injectable suspension, 7.5 mg every month, Sterile, Rx Only, Must be reconstituted…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tolmar, Inc.
FDA (openFDA drug enforcement)
Reported Sep 27, 2023
Perifix¿ / Epidural anesthesia set, medicated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 27, 2023
Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Humanrace
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 27, 2023
Power Snacks Honey Roasted Sunflower Kernels, Net Wt 1 oz; UPC 076500722025
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mount Franklin Foods LLC dba Azar Nut Co.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2023
Cequa (cyclosporine ophthalmic solution) 0.09%, 60 Single-Use Vials (6 pouches x 10 single-use vials (0.25 mL each)),…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sun Pharmaceutical Industries Inc.
FDA (openFDA drug enforcement)
Reported Sep 20, 2023
ASG-001; Ultrasound gel
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advance Medical Designs, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2023
Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Manufactured and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm LLC
FDA (openFDA drug enforcement)
Reported Sep 6, 2023
PORTEX 0.5u HYDROPHOBIC DISC FILTER, REF 002291 - Bacterial/Viral filter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2023
Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count Bottle, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Aug 30, 2023
Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075%, 5mL bottle, Imprimis NJOF, LLC. 1705 Route 46 West,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Imprimis NJOF, 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.