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 Oct 31, 2012
Synchron Systems Synchron Calibrator Multi Calibrator Diskettes, Part Number 442600. The SYNCHRON MULTI-CALIBRATOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Beckman Coulter Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only BiCNU manufactured by: Ben Venue Laboratories, Inc.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bristol-myers Squibb Company
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Oct 24, 2012
Diet Crush Orange Soda, 12 oz cans
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bottling LLC dba Pepsi Beverages Company
FDA (openFDA food enforcement)
Reported Oct 24, 2012
Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Net Wt 36 FL OZ (1.06 L) upc 73321-04418 J & J Snack Foods Corp.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.J & J Snack Foods Corporation
FDA (openFDA food enforcement)
Reported Oct 24, 2012
Frozen Red Cod Fillet (Red Snapper) Individually Quick Frozen was labeled and identified as Snapper FILL IQF…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Southwind Foods LLC dba Great American Seafood Imports Co.
FDA (openFDA food enforcement)
Reported Oct 17, 2012
Triage TOX Drug Screen Panel, Model# 94400. Product Usage: The Triage TOX Drug Screen is a fluorescence immunoassay…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Da Vinci Pesto Genovese with basil and pine nuts Net Wt. 10 oz. (283 g) Distributed by World Finer Foods, Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Finer Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 3, 2012
Fentanyl Transdermal System, 100 mcg/h, each transdermal system contains: 10 mg fentanyl and 0.4 mL alcohol USP, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Actavis
FDA (openFDA drug enforcement)
Reported Oct 3, 2012
UltraFlow HPC Flow Directed Micro Catheter, Model # 105-5065. Product Usage: The UltraFlow HPC Flow Directed Micro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics Inc., dba Ev3 Neurovascular
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 3 mL in 12 mL Single Use Syringe, Rx only, List no.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Amsino Medical USA
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Bard Ventralight ST Mesh. - Ellipse 8" x 10" (20.3 cm x 25.4 cm) Product Code 5954810. The Bard Ventralight ST Mesh is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Davol, Inc., Subs. C. R. Bard, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Polar Dressing, Knee/MU/Shldr Intelli-Flo-Breg, PN 10630 Used with cold therapy pads to provide insulation barrier…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breg Inc., An Orthofix Company
FDA (openFDA device enforcement)
Reported Sep 12, 2012
CLIF Bar Brand Coconut Chocolate Chip CLIF Bars, 6-pack boxes, UPC: 7-22252-66030-5 Product is manufactured by Harlan…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clif Bar And Company
3 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 12, 2012
Little Remedies For Tummys, Stimulant Laxative (sennosides) Drops, 1 FL OZ (30 mL), Dist. by Medtech Products Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtech Products, Inc.
FDA (openFDA drug enforcement)
Reported Sep 5, 2012
Leflunomide tablets, 10 mg, a) 30-count bottle (NDC 60505-2502-1), b) 1000-count bottle (NDC 60505-2502-3), Rx only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Corp.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 5, 2012
Capex Shampoo (fluocinolone acetonide), Topical Shampoo, 0.01%, Rx only, For Topical Use Only, 4 fl oz in a 6 oz…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Galderma Laboratories, LP
FDA (openFDA drug enforcement)
Reported Sep 5, 2012
Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory Packs (also commonly known as convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SRI Surgical
FDA (openFDA device enforcement)
Reported Aug 22, 2012
Derma-Smoothe/FS (Fluocinolone Acetonide) 0.01% Topical Oil (Scalp Oil), 4 fl oz (118.28mL) bottle, Rx only, FOR…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hill Dermaceuticals, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 22, 2012
13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nico Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 22, 2012
System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Aug 15, 2012
AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. --- Size: 5F; Length: 100cm; designed to accept…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Worldwide Headquarters
FDA (openFDA device enforcement)
Reported Aug 15, 2012
djo surgical Screw 6.5 mm, Sz 25mm, low profile. Product is intended for the fixation of the acetabular shell or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Aug 15, 2012
HYDROmorphone HCl Injection, USP, 1 mg/mL, 1 mL fill in a 2.5 mL Carpuject prefilled cartridge unit, packaged in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
FDA (openFDA drug enforcement)
Reported Aug 8, 2012
Dr. Reddy's Amlodipine Besylate and Benazepril Hydrochloride 5 mg*/20 mg, 500 Capsules, Rx only, Mfd. By: Dr. Reddy's…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Reddy's Laboratories, Inc.
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.