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. 1,736 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,736 in last 12 months

Showing 4286142880 of 49,150 recalls

Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Express Dry Seal ATS (Autotransfusion) Blood Recovery System Chest...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Atrium Medical Corporation

Recalled Item: Atrium Ocean Water Seal Chest Drain ATS (Autotransfusion) Blood Recovery...

The Issue: Chest Drain tubing of of the ATS Blood recovery may leak or disconnect

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Conset Infusion Set with 60cm tubing & 6mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2013· Asante Solutions, Inc.

Recalled Item: Asante Comfort Infusion Set with 60cm tubing & 13mm cannula packaged in...

The Issue: Reports of the infusion tubing disconnecting from the connector, resulting...

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

Class II — Potential Health HazardOngoing
FoodNovember 19, 2013· Nexgen Pharma, Inc.

Recalled Item: PCC Recalled by Nexgen Pharma, Inc. Due to Nexgen Pharma Inc. is recalling...

The Issue: Nexgen Pharma Inc. is recalling one lot of Woman's Once Daily vitamin...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Strata II Shunt Assembly Kit Recalled by Medtronic Neurosurgery...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 4-7 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Lite Blood Glucose Test Strips Recalled by Abbott Diabetes Care,...

The Issue: Certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 2-3 Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Blood Glucose Test Strips Recalled by Abbott Diabetes Care, Inc....

The Issue: Certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 1-1.5 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 4-7 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Delta Shunt Assembly Kit with Bioglide Small Recalled by Medtronic...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: CSF-Unitized Shunt Recalled by Medtronic Neurosurgery Due to Medtronic...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 2-3 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 1-1.5 HP Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing