All recall categories

Recalls distributed in Nebraska

These notices name Nebraska in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,352 stored notices name Nebraska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Nebraska too — those are in the archive.

Food

Reported Nov 6, 2013

the Snack Artist BBQ Flavored Potato Chips, Net Wt. 10 oz. (283 g), UPC 21130-29106. Distributed by Safeway, Inc.…

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

Barrel O' Fun Snack Foods Co.

FDA (openFDA food enforcement)

Food

Reported Nov 6, 2013

P.F. Chang's Home Menu, Pork & Leek Dumplings, frozen, packaged in 12.5 oz bags. UPC: 0 36200 21215 8

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

Conagra Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2013

Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…

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

DePuy Spine, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2013

pocH-100i; sysmex; Automated Hematology Analyzer; 7.3" x 13.8" x 18.1" / 30.8 lbs.; Sysmex Corporation; 1-5-1…

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

Sysmex America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2013

FSE Image Upgrade Kit, Catalog # 92019C This kit is used to install and/or upgrade software used with the EVOLIS…

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

Bio-Rad Laboratories

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2013

Frozen Sliced Carrots, packaged in 2 lbs. bag, sold under Simplot Classic brand. The UPC is 0 71179 1846 3 1. The…

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

Norpac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2013

Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…

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

Getinge Disinfection

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2013

Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R) Reagent Cartridge Lot 11349BB The Urinary /…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

SHOPKO Waterproof Adhesive Pads Antibacterial. Used for covering minor cuts, scrapes and burns.

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

Aso, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia Full Field Digital…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2013

Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

BD Epilor Syringe BD Franklin Lakes, NJ 07417 BD EDC Laagstraat 57, B-9140 Temse-Belgium The Epilor syringe is used in…

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implantable and indicated…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 2, 2013

Almond Biscotti, 1 oz. and 0.5 oz. wrapped in plastic, with "Enjoy By dates prior to 091614, manufactured by…

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

Semifreddi's Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 2, 2013

Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060-1834 USA…

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2013

Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…

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

Stryker Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

GE Healthcare, CARESCAPE Monitor B850. Intended for use in multiple areas within a professional healthcare facility.

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

GE Healthcare, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2013

Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2013

ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system…

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

Rauland-Borg Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2013

Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measurement of axial eye length.

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

Sonogage 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.