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. 1,095 recalls have been distributed to Nevada in the last 12 months.
Showing 8981–9000 of 28,334 recalls
Recalled Item: VIDAS SARS-COV-2 IgG Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...
The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Measles IgG (MSG) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Clostridium Difficile GDH Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS DEX@ Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Mumps IgG (MPG) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Lyme IgM II (LYM) Recalled by bioMerieux, Inc. Due to bioMerieux has...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation/RayPlan versions 4 - 11A Recalled by RAYSEARCH LABORATORIES AB...
The Issue: An issue where the combined density in a dose grid voxel partially covered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS TOXO IgG Avidity (TXGA) Recalled by bioMerieux, Inc. Due to bioMerieux...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The da Vinci Xi and X surgical systems (IS4000 and Recalled by Intuitive...
The Issue: Incorrect expiration date on its package labeling (shipper box and inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Li-Ion Battery Pack Recalled by Datascope Corp. Due to A...
The Issue: A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC PneumoLiner device Recalled by Olympus Corporation of the Americas Due...
The Issue: Due to manufacturing error, the Pneumoliner Bag Distal Tab that exits the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The firm has confirmed the potential for ADVIA Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR...
The Issue: 7FR Percutaneous Thrombolytic Device (PTD) Inner lumen (orange) detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5MMX165MM CANNULATED SCREW Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The product label incorrectly indicated that the screws are fully threaded,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.