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. 2,347 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,347 in last 12 months

Showing 4672146740 of 49,150 recalls

DrugNovember 21, 2012· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluorouracil Topical Cream USP Recalled by Taro Pharmaceuticals U.S.A., Inc....

The Issue: Product Lacks Stability: Out-of-specification (OOS) results were observed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 21, 2012· Remel Inc

Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...

The Issue: Boxes labeled as CIP5 may contain cartridges of AMP5.

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Str Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Angled Wire The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2012· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare is aware of a potential safety issue associated with the use...

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

Class III — Low RiskOngoing
DrugNovember 19, 2012· Ascend Therapeutics Inc

Recalled Item: EstroGel (estradiol gel) 0.06% Recalled by Ascend Therapeutics Inc Due to...

The Issue: Defective Container: Pump head detaching from the canister unit upon removal...

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

Class III — Low RiskOngoing
Refund
FoodNovember 19, 2012· Capital City Fruit Co.

Recalled Item: Cherry tomatoes packaged in 1 pint clear Recalled by Capital City Fruit Co....

The Issue: The recalled cherry tomatoes are associated with the Rio Queen Citrus, Inc....

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 19, 2012· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Intersept Custom Tubing Pack with or without coating ( Recalled by...

The Issue: Medtronic is initiating an Urgent Medical Device Customer Notification. We...

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

Class II — Potential Health HazardOngoing