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. 1,132 recalls have been distributed to Nebraska in the last 12 months.
Showing 1361–1380 of 49,150 recalls
Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...
The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FERNO POWER X2 POWERED AMBULANCE COT Recalled by Ferno-Washington Inc Due to...
The Issue: The fastening post hardware could loosen allowing the fastening post to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENACIO Pump without InhibiZone Recalled by Boston Scientific Corporation...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TH1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...
The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...
The Issue: Potential that the measured value may be smaller than the actual area.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500...
The Issue: The device either indicated a failure of the piston ventilator before use or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600...
The Issue: The device either indicated a failure of the piston ventilator before use or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...
The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Chemo Lock Universal Vented Vial Spike Recalled by ICU Medical,...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 21" Ext Set w/ChemoLock Port Recalled by ICU Medical, Inc. Due...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 6.5" Bag Spike w/ChemoLock Port Additive Port Recalled by ICU...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.