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. 2,684 recalls have been distributed to Nevada in the last 12 months.
Showing 8761–8780 of 28,334 recalls
Recalled Item: Heel Snuggler Recalled by Philips North America Llc Due to After the device...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Infant Heel Warmer Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infa-Therm Transport Mattress Recalled by Philips North America Llc Due to...
The Issue: After the device was cleared by the FDA, Philips made changes to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura Xper Recalled by Philips North America Llc Due to Due to a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Radiotherapy System - System Label: "*** by Medical, Inc. Due to Due...
The Issue: Due to dose discrepancy when delivering a plan to a patient in a Non-HFS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBB-06 Hemodialysis Delivery System Recalled by Nikkiso Ltd - Shizuoka Plant...
The Issue: Device lacks premarket approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Pro Tibial Preparation Tray Recalled by Howmedica Osteonics Corp....
The Issue: Triathlon Pro Tibial Preparation Tray may have been kitted with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error which affects Sensis Vibe Hemo, Sensis and Sensis Vibe Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Multi-Access Port Catheter Recalled by Avanos Medical, Inc. Due to...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Multi-Access Port (MAP) Catheter Recalled by Avanos Medical, Inc....
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BALLARD* Seal Cassette Replacement MAP - BALLARD* Seal Cassette Replacement...
The Issue: Product was distributed with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack Recalled...
The Issue: Lower than expected results for VITROS¿ Immunodiagnostic Products TSH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electri-Cool II Portable Cold Therapy Unit Recalled by Gentherm Medical, LLC...
The Issue: This recall has been initiated to provide a labeling update with revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar) Recalled by...
The Issue: The U-channel sheaths may cause damage to ProACT implant devices when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIRION EMBOLIC PROTECTION SYSTEM Recalled by Cardiovascular Systems Inc Due...
The Issue: Under certain circumstances, the WIRION filter assembly may become difficult...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAcube Connect MDx Recalled by Qiagen Sciences LLC Due to During the "Load...
The Issue: During the "Load tip racks and enzymes" step of the run set-up, the info...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS-Computed tomography system Model 8098027 Recalled by...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...
The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.