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. 2,551 recalls have been distributed to Nevada in the last 12 months.
Showing 18861–18880 of 28,334 recalls
Recalled Item: Fresenius 2008T Series Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008K Series : Hemodialysis System Recalled by Fresenius Medical...
The Issue: When the UF Rate, Goal or Time is adjusted using the up and down arrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Negative bias with IMMULITE¿ /IMMULITE¿ 1000 Third Generation PSA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoDELFIA¿ Plate Processor Recalled by PerkinElmer Health Sciences, Inc....
The Issue: AutoDELFIA System with Version 3.0 Software: Potential plate loading failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...
The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...
The Issue: There is a potential for biased results to be generated over the 10 day...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: iOS and Android: Under certain conditions the affected app versions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...
The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM Recalled...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension AMM (DF119)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...
The Issue: The product was not functioning as intended. The ventilation to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.