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. 2,595 recalls have been distributed to Nevada in the last 12 months.
Showing 17641–17660 of 28,334 recalls
Recalled Item: Plum 360 Infusion System Recalled by ICU Medical Inc Due to Potential for...
The Issue: Potential for the Connectivity Engine Module of the affected unit to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArjoHuntleigh Flowtron ACS900 Recalled by Arjo, Inc. dba ArjoHuntleigh Due...
The Issue: Reports of the device failure involving delivering continuous pressure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...
The Issue: Manufacturing process used to assemble the circuit board may result in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...
The Issue: Manufacturing process used to assemble the circuit board may result in some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...
The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...
The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...
The Issue: A small number of customer observations were recently received which related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...
The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...
The Issue: This recall has been initiated due to a potential malfunction of the photo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.