Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,807 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,807 in last 12 months

Showing 4042140440 of 49,150 recalls

Medical DeviceOctober 9, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur (including ) Professional use in a laboratory for Recalled by...

The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Trumpf Medical Systems, Inc.

Recalled Item: TITAN Operating Room Table Patient positioning during surgery Recalled by...

The Issue: Unintended movement of the operating table during surgical cases due to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur XP Immunoassay System (including ) Professional use in...

The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2014· Cynosure, Inc.

Recalled Item: Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System...

The Issue: If the laser system is turned on and the user adjusts, installs or removes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Ad-Tech Medical Instrument Corporation

Recalled Item: Box Label: 3 mm Cueva Electrode Kit Recalled by Ad-Tech Medical Instrument...

The Issue: The recall has been initiated due to concerns that the applicator wand may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SmartLife Small Aseptic Housing Rx Only The Recalled by Stryker...

The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker SmartLife Large Aseptic Housing Rx Only The Recalled by Stryker...

The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 8, 2014· Lotte International America Corp (LA Branch)

Recalled Item: Lotte European Waffle Recalled by Lotte International America Corp (LA...

The Issue: Lotte International is recalling the Lotte Waffles because it contains...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 8, 2014· Teva Pharmaceuticals USA

Recalled Item: DEXTROAMPHETAMINE SACCHARATE Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 7, 2014· Zee Medical Products Inc

Recalled Item: ZEE Aspirin 325mg - 24 tablets in single dose packets Recalled by Zee...

The Issue: Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2014· Zimmer, Inc.

Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...

The Issue: Affected product did not undergo heat treatment hardening step leading to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mortara Instrument, Inc

Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...

The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7008 Part Number: MRI-08 MRI-Boot Product Usage: Radio...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Recalled by...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay Systems Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing