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 Dec 10, 2025
Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Genepro Protein, Inc.
FDA (openFDA food enforcement)
Reported Dec 3, 2025
The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Magellan Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 26, 2025
Klarity-C Drops (Cyclosporine) 0.1%, Preservative-Free Sterile Ophthalmic Emulsion, This is a compounded drug, Office…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Imprimis NJOF, LLC
FDA (openFDA drug enforcement)
Reported Nov 26, 2025
OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
FDA (openFDA device enforcement)
Reported Nov 12, 2025
Amoxicillin and Clavulanate Potassium for Oral Suspension USP, 200 mg/28.5 mg per 5mL, 100 mL (when reconstituted), Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teva Pharmaceuticals USA, Inc.
FDA (openFDA drug enforcement)
Reported Nov 3, 2025Updated Aug 26, 2026
Otsuka ICU Medical LLC recalls ICU Medical 20 mEq Potassium Chloride Injection due to Potential for Potassium chloride overdose: 20 mEq Potassium Chloride…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Otsuka ICU Medical LLC
FDA (recalls & safety alerts)
Reported Oct 22, 2025
Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.IntegraDose Compounding Services LLC
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 90 Tablets per bottle, Rx Only, Manufactured for Accord…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accord Healthcare, Inc.
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
Artegraft Collagen Vascular Graft. Model/Catalog/Part Numbers: AG630M, AG636M, AG730M, AG740M, AG845M. The Artegraft is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LeMaitre Vascular, Inc.
FDA (openFDA device enforcement)
Reported Oct 8, 2025
AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 8, 2025
Orwashers brand Soho Sourdough XL Batard; contains: wheat; 6-46.4oz PIECES PER CASE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oven Artisans LLC
FDA (openFDA food enforcement)
Reported Oct 1, 2025
READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medline Industries, LP
FDA (openFDA drug enforcement)
Reported Sep 30, 2025
Abdallah Inc. recalls Lunds & Byerlys Chocolate candy with nuts. due to Due to a mislabeled allergen, cashews
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Abdallah Inc.
FDA (recalls & safety alerts)
Reported Sep 24, 2025
Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascend Laboratories, LLC
FDA (openFDA drug enforcement)
Reported Sep 17, 2025
Ultra Violette, Velvet Screen SPF 50, Blurring Mineral Skinscreen, Zinc Oxide 22.75%, a) 15 mL, 0.5 fl. oz. per tube,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grace & Fire Pty Ltd.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Sep 10, 2025
Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boothwyn Pharmacy LLC
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 10, 2025
KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immunocore, LLC
FDA (openFDA drug enforcement)
Reported Aug 27, 2025
7up Zero Sugar Tropical Soda, 12 FL OZ (355 mL) aluminum cans, packaged in 12 pack cardboard cartons labeled as 7up…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Buffalo Rock Company Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2025
Unichem Pharmaceuticals recalls Unichem Pharmaceuticals Cyclobenzaprine Hydrochloride Tablets USP 10 mg due to Device & Drug Safety – Mislabel
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Unichem Pharmaceuticals
FDA (recalls & safety alerts)
Reported Aug 20, 2025
Zvu Anorectal Manometry Procedure Kit, REF: HRAM-PROC-10
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Diversatek Healthcare
FDA (openFDA device enforcement)
Reported Aug 20, 2025
Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEE INS, 4L 16MM, VE Model/Catalog Number:…
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 Aug 20, 2025
Levoxyl (levothyroxine sodium tablets, USP), 50 mcg, 100-count bottle, Rx only, Distributed by: Pfizer Inc., New York,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pfizer
FDA (openFDA drug enforcement)
Reported Aug 20, 2025
Soda Biscuit (Rye Flavor), Net Wt: 360g/12.07oz; Shelf life: 10 months; Manufacturer: Zhejiang Dinggian Industrial Co.,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Shang Hao Jia, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imprimis NJOF, LLC
1 more product in this recall
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.