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. 2,479 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,479 in last 12 months

Showing 2050120520 of 49,150 recalls

Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2019· Roche Diabetes Care, Inc.

Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...

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

Class II — Potential Health HazardOngoing
DrugSeptember 27, 2019· Arbor Pharmaceuticals Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Arbor Pharmaceuticals Inc. Due...

The Issue: Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP Recalled by Taro Pharmaceuticals...

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP may have small...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 27, 2019· Images Unlimited Products, dba Cellect Products

Recalled Item: CELLECT brand and ESSENTIALS FACTOR Cell Synergy brand Unflavored Powdered...

The Issue: Product contains unsafe levels of Arsenic and Lead

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

Class II — Potential Health HazardOngoing
Refund