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. 2,108 recalls have been distributed to Nebraska in the last 12 months.
Showing 661–680 of 49,150 recalls
Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...
The Issue: Customer complaints of Pressio monitor rebooting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted Recalled by...
The Issue: Products do not declare milk in the Contains statement or the ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lava Bun with Green Tea Flavor bright lime green packaging Recalled by Prime...
The Issue: Products do not declare milk in the Contains statement or the ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...
The Issue: Potential for incomplete seal on header bag.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...
The Issue: Potential for incomplete seal on header bag.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...
The Issue: Potential for incomplete seal on header bag.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...
The Issue: Potential for incomplete seal on header bag.
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: Software version 5.10.1 and earlier contain anomalies that have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for incomplete seal...
The Issue: Potential for incomplete seal on header bag.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...
The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.