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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 37561–37580 of 49,150 recalls
Recalled Item: Ring Transjugular Intrahepatic Access Set Product Usage: The Ring...
The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1X1 Cleaving Tiles Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor RTPS Guiding Sheath Product Usage: The Flexor RTPS Guiding Recalled...
The Issue: Cook Inc. is initiating a voluntary recall of the Ring Transjugular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 550 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 200 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 365 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 150 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pull Reduction Device For 4.3mm Percutaneous Drill Guide Recalled by...
The Issue: Certain affected parts and lots of the Pull Reduction Devices may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm Recalled by...
The Issue: certain lots of the Titanium Recon Screws (6.5mm ) were found to contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.