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. 2,059 recalls have been distributed to Nebraska in the last 12 months.
Showing 3841–3860 of 28,140 recalls
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...
The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...
The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHO KNEE BAPTIST SOUTH PACK Procedure tray Catalog Number: BPKA49B...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R Recalled by American Contract...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S Recalled...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.