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. 2,562 recalls have been distributed to Nevada in the last 12 months.
Showing 18521–18540 of 28,334 recalls
Recalled Item: Fem IM Nail 16mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 25.5x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 18x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx46cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 24.0x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...
The Issue: A defective electrical component in the battery charging circuit in two lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.