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. 2,450 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,450 in last 12 months

Showing 2430124320 of 49,150 recalls

DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Valsartan Tablets USP Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine and Valsartan Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2018· Torrent Pharma Inc.

Recalled Item: Amlodipine Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 16, 2018· Medtronic Vascular

Recalled Item: Medtronic DxTerity(TM) TRA 5F Recalled by Medtronic Vascular Due to...

The Issue: Medtronic has determined that the French size indicator on the inner pouch...

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

Class III — Low RiskOngoing
Medical DeviceAugust 15, 2018· TriMed Inc.

Recalled Item: TriMed Olecranon Hook Plate Recalled by TriMed Inc. Due to The firm has...

The Issue: The firm has become aware that the angled-hole of certain semi-tubular...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System-For use in the in vitro quantitative Recalled...

The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System- (). For use in the in Recalled by...

The Issue: Potential for the VITROS 5600 Integrated System to dispense an insufficient...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...

The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...

The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Agilent Technologies, Inc.

Recalled Item: MassHunter Quantitative Analysis Software Recalled by Agilent Technologies,...

The Issue: When utilizing specific software versions of an LC/MS device, and Batch at a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2018· Permobil, Ab

Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...

The Issue: This correction decision has been made because of a potential failure of one...

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

Class II — Potential Health HazardOngoing