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. 2,439 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,439 in last 12 months

Showing 3008130100 of 49,150 recalls

Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arterial Line Kit with Sharps Safety Features and Maximal Barrier Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit. The...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow VPS Access Kit with Maximal Barrier Precautions for use Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow Pressure Injectable PICC Kit The Arrow International Pressure...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit The...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore multiple-lumen...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R) Recalled by...

The Issue: The large-bore two-lumen catheter permits venous access to the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High...

The Issue: The large-bore two-lumen catheter permits venous access to the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· G & W Laboratories, Inc.

Recalled Item: Ciclopirox Olamine Cream USP Recalled by G & W Laboratories, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: product lots packaged with an...

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: CLENZIderm M.D. Acne Treatment System Recalled by Valeant Pharmaceuticals...

The Issue: Discoloration.

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Fluocinonide Cream UPS Recalled by Taro Pharmaceuticals U.S.A., Inc. Due to...

The Issue: Cross contamination with other products: Certain lots of Fluocinonide Cream...

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

Class III — Low RiskOngoing
Refund
DrugMarch 17, 2017· Akorn, Inc.

Recalled Item: LATANOPROST OPHTHALMIC SOLUTION Recalled by Akorn, Inc. Due to Lack of...

The Issue: Lack of assurance of sterility: product was found to be empty, under-filled,...

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

Class II — Potential Health HazardOngoing
Refund