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. 2,613 recalls have been distributed to Nevada in the last 12 months.
Showing 15941–15960 of 28,334 recalls
Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Ingress of fluids into the device can affect various electronic circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...
The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...
The Issue: The devices may have been assembled with an internal component that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...
The Issue: The bottles are mislabeled with an incorrect part number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...
The Issue: Cross-contamination of samples has been reported when running the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...
The Issue: Possible transient electrical connection interruption between an HVAD System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...
The Issue: The diameter of the drill sleeve guide raw material was found to be under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...
The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...
The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...
The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...
The Issue: The firm has received 106 complaints of the device breaking in the patient's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...
The Issue: Device was marketed for uses outside the 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...
The Issue: After the Large Display returns from power save mode, it may not show an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.