Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. 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 Nevada in the last 12 months.
Showing 3821–3840 of 28,334 recalls
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: Abbott Proclaim DRG 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: KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B 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: LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X 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: ACL Recalled by American Contract Systems Inc Due to Ethylene Oxide/Ethylene...
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.
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 - 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: 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: HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I 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-Procedure Kit Catalog Number: SFAR60A 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: 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: 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: 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: 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: A610 Clinician Programmer (CP) Software Application (app) with the following...
The Issue: Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...
The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...
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: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.