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. 2,608 recalls have been distributed to Nebraska in the last 12 months.
Showing 9421–9440 of 28,140 recalls
Recalled Item: MYLA software. Used to manage microbiology test workflow from the Recalled...
The Issue: Software anomaly - Under certain conditions, unwanted alterations to results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...
The Issue: The firm has identified a potential for the backrest to become detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...
The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...
The Issue: Out of Specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...
The Issue: There is a potential risk of device contamination and patient infection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...
The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.