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. 2,689 recalls have been distributed to Nevada in the last 12 months.
Showing 6641–6660 of 28,334 recalls
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaOne Reusable Positioning Cannula 12mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaOne Reusable Positioning Cannula 8 mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software Recalled by...
The Issue: Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion System with software versions: R2.2.O Recalled by PHILIPS...
The Issue: Potential Loss of X-ray-When the full disk capacity is reached, X-Ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and...
The Issue: Potential for the spring to become loose and fall out of the device, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 11MM X Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System: ENDO SLED KNEE FEM COMP Recalled by Linkbio Corp. Due...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 13 Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13X58MM Item Recalled by...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP Recalled by Linkbio...
The Issue: Additional Label Warnings: Amendment / reinforcement of the Surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.