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.
Showing 30021–30040 of 49,150 recalls
Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...
The Issue: There have been five reports of graft thrombosis/occlusion during global...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...
The Issue: pegs shearing post-operatively
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...
The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilocarpine Hydrochloride Ophthalmic Solution 4% Recalled by Novartis...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Tablets Recalled by Sun Pharmaceutical Industries, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isopto Carpine (pilocarpine hydrochloride opthalmic solution) 4% Recalled by...
The Issue: Failed Impurities/Degradation Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Aerosol Recalled by...
The Issue: Defective Delivery System: Elevated number of units with out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...
The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Mylan Institutional, Inc. (d.b.a....
The Issue: Microbial Contamination of Non-Sterile Products: potential of an elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...
The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC)...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit. The large-bore...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.