All recall categories

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.

Medical devices

Reported Oct 19, 2016

TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biocompatibles U.K., Ltd.

FDA (openFDA device enforcement)

Drugs

Reported Oct 19, 2016

Marcaine 0.25% (bupivacaine HCl) injection, USP, 125 mg/50 mL (2.5 mg/mL), 50 mL Multiple-Dose Vial, Rx only, Hospira,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hospira Inc., A Pfizer Company

1 more product in this recall

FDA (openFDA drug enforcement)

Food

Reported Oct 19, 2016

Supermoms Kitchen Roast Beef & Cheddar Melt, Net Wt. 3.7 oz (105g). Keep Refrigerated. UPC 63913-94236

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Northern Tier Bakery

FDA (openFDA food enforcement)

Medical devices

Reported Oct 19, 2016

Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2016

SENSAR Foldable IOL with OptiEdge Design, Model No. AR40e The product is indicated for implantation for the visual…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Medical Optics Inc. (AMO)

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2016

Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 28, 2016

EAT Barbeque Zero to Hero, a Sweet Rub, packaged in 6.5oz bottles (mislabeled). The responsible firm named on the label…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Old World Spices & Seasonings Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2016

FPS 35mm x 3.5 mm non-locking screw

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho Solutions Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2016

3.5mm Bowed Locking Compression Femur Plates, 14 hole Orthopediatrics PediLoc Locking Plate System comes in sets that…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OrthoPediatrics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 28, 2016

Fresh Food Market Cranberry Chicken Salad, UPC 207063-4XXXX, various package sizes. Product sold both from bulk service…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Sep 21, 2016

Whole Food Market Thai Shrimp Salad Serving Size 8 oz. Distributed by Whole Foods Market Englewood Cliffs NJ 07632 UPC…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Whole Foods Market Northeast Regional Office

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2016

Arterial Line Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 7, 2016

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Clinique International

5 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Sep 7, 2016

Euro Custard Cake, Plastic wrapped cardboard container (Net Wt. 7.20 oz.)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Eastland Food Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2016

Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement provides two separate, pre-measured and sterilized…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2016

The Cheese & Berries Danish was labeled Pleasant Hill Ovens, Cheese Danish, Artificial Flavored, Net WT 5.0 OZ (142 g),…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Northern Tier Bakery (dba\ Super Mom's)

FDA (openFDA food enforcement)

Drugs

Reported Aug 31, 2016

Amoxicillin for Oral Suspension USP, 400 mg/ 5 mL, 50 mL bottle, Rx only, Manufactured In Canada by: Teva Canada…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teva North America

FDA (openFDA drug enforcement)

Meat & poultry

Reported Aug 3, 2016

Grossglockner Inc. Recalls Pork Products Due To Misbranding

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Grossglockner Inc.

USDA FSIS

Medical devices

Reported Aug 3, 2016

Endotine Transbleph 3.5 (CFD-080-0167)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MicroAire Surgical Instruments, LLC

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 1, 2016

Michael Angelo's Gourmet Foods, Inc. Recalls Shrimp Scampi and Meat Lasagna Products Due To Misbranding and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Michael Angelo's Gourmet Foods Inc.

USDA FSIS

Medical devices

Reported Jul 20, 2016

Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K 810675, product code DQX, Device Listing…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jul 13, 2016

fentaNYL citrate in 0.9% Sodium Chloride Injection, 10 mcg/1 mL (10 mcg/mL), in 1 mL Syringe, Rx Only, Cantrell Drug…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Cantrell Drug Company

12 more products in this recall

FDA (openFDA drug enforcement)

Meat & poultry

Reported Jul 13, 2016

Michael Angelo's Gourmet Foods, Inc. Recalls Shrimp Scampi Products Due To Misbranding and Undeclared Allergens

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Michael Angelo's Gourmet Foods Inc.

USDA FSIS

Medical devices

Reported Jun 29, 2016

EV3 EverFiex" Self-expanding Peripheral Stent System, Sterilized using Ethylene Oxide, Rx Only, PRB35-08-040-080. The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ev3, Inc.

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.