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.
Reported Aug 20, 2014
Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For use in conjunction with the Medtronic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 6, 2014
MC-500 Multicolor Laser Photocoagulator; Distributed by NIDEK Inc. Manufactured by NIDEK CO., Ltd, Japan. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Original Silk Light Soymilk Half Gallon, Distributed by WhiteWave Foods Broomfield, Colorado 80021, UPC 0 25293 60101 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.White Wave Foods, Inc.
FDA (openFDA food enforcement)
Reported Jul 30, 2014
AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Corp.
FDA (openFDA device enforcement)
Reported Jul 30, 2014
RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2014
MK5 NX Controller--Wheelchair controller
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Jul 30, 2014
Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
10 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2014
Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direct Patient…
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)
Reported Jul 30, 2014
Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2014
ACL TOP (Base), automated coagulation laboratory instrument.
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)
Reported Jul 23, 2014
Velveeta Original Pasteurized Ripe Cheese Product sold under the Kraft brand and individually wrapped in plastic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
FDA (openFDA food enforcement)
Reported Jul 23, 2014
There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NW Nutritional Foods LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 23, 2014
Thermo Scientific VersaTREK REDOX 1, Ref 7102-44, 80ml with Stir Bar (O2 aerobic), 50 bottles/box, IVD. The firm name…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Jul 23, 2014
Coat-A-Count Direct Androstenedione, SMN 10381049, Catalog Number TKAN1. Siemens Healthcare Diagnostics
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 23, 2014
e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oregon Freeze Dry, Inc.
FDA (openFDA food enforcement)
Reported Jul 16, 2014
The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
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.