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 2780127820 of 49,150 recalls

Medical DeviceAugust 9, 2017· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module model 8100 manufactured between November 2011 and March...

The Issue: The recalling firm has received reports of increased or decreased flows that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2017· LifeCell Corporation, A Wholly Owned Subsidiary of Allergan PLC

Recalled Item: REVOLVE ADVANCED ADIPOSE SYSTEM Recalled by LifeCell Corporation, A Wholly...

The Issue: Presence of bacterial endotoxins levels above the acceptable limit

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2017· International Laboratories, Inc.

Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...

The Issue: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 7, 2017· Michele's Granola LLC

Recalled Item: Michele s Toasted Muesli Recalled by Michele's Granola LLC Due to Potential...

The Issue: The product has been recalled due to the potential to be contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 7, 2017· Merge Healthcare, Inc.

Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...

The Issue: The software is not identifying the patient as having atypical hyperplasia,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Right Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Left Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Stemmed Tibial Provisional Size H Left Recalled by Zimmer Biomet,...

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Cemented Tibial SZ PLT Size H Right Recalled by Zimmer Biomet, Inc....

The Issue: There is a potential for intermittent cracks in the raw material batch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Covidien LLC

Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...

The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2017· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...

The Issue: During the rework process for the April 17, 2017, field action, it was...

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

Class II — Potential Health HazardOngoing