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. 1,106 recalls have been distributed to Nebraska in the last 12 months.
Showing 2681–2700 of 49,150 recalls
Recalled Item: IceSeed 1.5 CX NEEDLE OUS Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand: Recalled by Baxter...
The Issue: There were customer reports of devices which experienced battery-related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE OUS Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...
The Issue: The associated product labeling does not adequately provide compatibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled by...
The Issue: A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX NEEDLE US Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn CP150 Electrocardiograph: Recalled by Baxter Healthcare...
The Issue: There were customer reports of devices which experienced battery-related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE US Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phasor Drill Recalled by Phasor Health, LLC Due to Drill for use in...
The Issue: Drill for use in neurosurgical procedures may have a reverse battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESTATION 650C A2 Recalled by GE Medical Systems China Co.,...
The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation 650 SE Recalled by GE Medical Systems China Co.,...
The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.