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. 2,680 recalls have been distributed to Nevada in the last 12 months.
Showing 9461–9480 of 28,334 recalls
Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...
The Issue: There is a potential risk of device contamination and patient infection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...
The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235- designed to produce and deliver a proton beam Recalled by Ion...
The Issue: Users may be misled by the popup message displayed by the Proton Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...
The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut R Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO PLUS Delivery Catheter System Recalled by Medtronic...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...
The Issue: The IndiGo power cord might wear during use which could lead to its damage,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...
The Issue: There is a potential for 15% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...
The Issue: Due to a design issue, inflation syringe handle separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lingen SAMPLE Disposable Virus Sampling Kit pack Recalled by Mercedes...
The Issue: No 510(k) clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.