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. 933 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
933 in last 12 months

Showing 43801–43820 of 49,150 recalls

DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Watson Laboratories Inc

Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Watson Laboratories Inc Due...

The Issue: Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· AmeriSource Bergen

Recalled Item: Ifosfamide Injection 3g/60 mL Recalled by AmeriSource Bergen Due to...

The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· AmeriSource Bergen

Recalled Item: Ifosfamide Injection 1g/20mL Recalled by AmeriSource Bergen Due to...

The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Lamotrigine Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 13, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2013· CooperSurgical, Inc. D.B.A. Lone Star Medical Products

Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...

The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...

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

Class II — Potential Health HazardOngoing
FoodSeptember 12, 2013· Dutch Valley Food Development Inc.

Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...

The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 12, 2013· Dutch Valley Food Development Inc.

Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...

The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 12, 2013· Maquet Medical Systems USA

Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...

The Issue: It has come to the attention of MAQUET that in certain rare instances, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2013· Beckman Coulter Inc.

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

The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· SonoSite, Inc.

Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...

The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Harvest Technologies Corporation

Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...

The Issue: Potential for leur connector to leak or have cracks.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...

The Issue: There is a potential issue on running Artis systems running software VC1x...

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

Class II — Potential Health HazardOngoing