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. 2,439 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,439 in last 12 months

Showing 2674126760 of 28,140 recalls

Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 8000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Abbott Laboratories, Inc

Recalled Item: Clinical Chemistry Phenobarbital Recalled by Abbott Laboratories, Inc Due to...

The Issue: Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100-BGM Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Biomet, Inc.

Recalled Item: Biomet Offset Tibial Tray 2.5 mm Adaptor Recalled by Biomet, Inc. Due to...

The Issue: Biomet investigation identified that the square end of the offset tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· EEG Info

Recalled Item: EEG NeuroAmp Recalled by EEG Info Due to Mislabeling

The Issue: EEG Info, Inc. is recalling the EEG Neuroamp device because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· GE Healthcare It

Recalled Item: GE Centricity PACS Workstation Recalled by GE Healthcare It Due to While...

The Issue: While merging exams in a test instance, merges carry forward in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: This notice is being provided in follow up to the field correction initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur CA 19-9 250 Test 10491244 50 Recalled by...

The Issue: Operating range of the ADVIA Centaur systems is 18C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Digitoxin (DGTN) 250 Test 09046419 50...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular System (TCVS) has received reports of a situation...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Theophylline 2 (THE02) 250 Test 08838753...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing