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. 2,612 recalls have been distributed to Nebraska in the last 12 months.
Showing 8141–8160 of 28,140 recalls
Recalled Item: Centricity Universal Viewer Zero Footprint Client Recalled by GE Healthcare,...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Web Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardiology CA1000 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS RA1000 Recalled by GE Healthcare, LLC Due to Potential for...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRMap" Catheter Recalled by Abbott Due to Incorrect product labeling.
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TEG 5000 Functional Fibrinogen Reagent Recalled by Haemonetics Corporation...
The Issue: Due to a shift in the citrated blood range for a normal population, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Wet -Field Eraser Recalled by Beaver Visitec International, Inc. Due to...
The Issue: Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In-Line ventilator adaptor Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential of reduced oxygenation or pneumothorax/barotrauma to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control...
The Issue: Software issue, resuming an interrupted treatment will result in swap of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Back up batteries in Avance CS2 and Avance CS2 Pro Recalled by GE...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Field replacement back up batteries distributed on or after April 1 Recalled...
The Issue: Backup batteries can fail earlier than their estimated life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V2.x. Recalled by CardioTek BV Due to Device...
The Issue: Device did not pass electrical safety testing for adequate insulation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Start-up time for the flow rate range greater than 50 ml/hr, and less than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Ivenix, Inc. Due to Downstream...
The Issue: Downstream occlusion alarm is sometimes immediately followed by a pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper...
The Issue: Part (A-rubber) intended for a different model of gastrointestinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonovideoscope Model CF-H180AL Recalled by Olympus Corporation of the...
The Issue: A (Camera unit) CCD intended for a different model of colonoscope may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to There is the potential that...
The Issue: There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Synergy Washer/Disinfector Recalled by Steris Corporation Due to...
The Issue: The firm identified that when the electrical contactor component in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.