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. 2,659 recalls have been distributed to Nevada in the last 12 months.
Showing 11021–11040 of 28,334 recalls
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...
The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with 4mm Adapter - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Paddles Recalled by Philips North...
The Issue: The periodic Paddle Checks recommended in the Instructions for Use for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Sterilizable Defibrillator Paddles Recalled by Philips North...
The Issue: The periodic Paddle Checks recommended in the Instructions for Use for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nexiva Closed IV Catheter System Dual Port (20 GA Recalled by Becton...
The Issue: Dull/blunt needles within the IV Catheter System may lead to missed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR Coils The MR Coil is intended to be used Recalled by Invivo Corporation...
The Issue: The labels have been mistakenly printed with an IPX1 rating symbol. IPX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301023 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #650301018 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Model #65021652 Recalled by Medline Industries Inc Due to Non-sterile...
The Issue: Non-sterile kits intended to be sterilized prior to use were sold to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.