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 Apr 15, 2026
XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.XTANT Medical Holdings, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2026
Levothyroxine Sodium Tablets USP 150 mcg, 1000 Tablets bottle, 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 Mar 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winder Laboratories, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KOB GmbH
FDA (openFDA device enforcement)
Reported Mar 4, 2026
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 25, 2026
Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centinel Spine, Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported Feb 11, 2026
spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTEN - NO MSG - NO SOY NO PRESERVATIVES - NO WHEAT NO SUGAR -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Organic Spices, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 28, 2026
Thyroid, USP, Rx only, Net Wt: 0.50kg, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Specialty Process Labs LLC
FDA (openFDA drug enforcement)
Reported Jan 28, 2026
Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zydus Pharmaceuticals (USA) Inc.
FDA (openFDA drug enforcement)
Reported Jan 21, 2026
BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip, Coated, Female REF: RTU14F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hangzhou Bever Medical Devices Co., Ltd.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
BIOSURE HA SCREW, 6MM x 20 MM. Threaded metallic bone fixation fastener.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2025
Cisatracurium Besylate Injection USP, 10 mg/5 mL* (2mg/mL), 10 x 5 mL Single-dose Vials per Carton, Rx Only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Somerset Therapeutics LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 17, 2025
ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
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)
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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.