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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 2361–2380 of 28,334 recalls
Recalled Item: Baxter Solution Set with Duo-Vent Spike Recalled by Baxter Healthcare...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Clearlink System Solution Set with Duo-Vent Spike Recalled by Baxter...
The Issue: Specific lots of Solution Sets with Duo-Vent Spike have the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number:...
The Issue: Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breathe Technologies Recalled by Baxter Healthcare Corporation Due to There...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Recalled by Baxter Healthcare Corporation Due to There is an...
The Issue: There is an issue with the ventilator battery charger that could lead to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each) Recalled by...
The Issue: During the assembly of the cartridge to its connecting body part, the valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KARL STORZ - ENDOSKOPE Recalled by Karl Storz Endoscopy Due to Scope IFUs...
The Issue: Scope IFUs contain a reprocessing modalities that have not been reviewed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.