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.
Showing 20281–20300 of 28,140 recalls
Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...
The Issue: During an FDA inspection it was found that the products are marketed without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...
The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...
The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Assays: Direct HDL Cholesterol (AHDL) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Navigation O-arm 02 surgical x-ray imaging system Recalled by...
The Issue: Review of on-system electronic product labeling and Instr uctions for Use in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Assay: Direct HDL Cholesterol (D-HDL) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA CHEMISTRY TRIGLYCERIDES_2 (TRIG_2) REAGENT & ADVIA CHEMISTRY...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Assay: Uric Acid and Uric Acid Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Assays: Uric Acid (URCA) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Assays: Triglycerides (TGL) Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.