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. 2,510 recalls have been distributed to Nevada in the last 12 months.
Showing 24801–24820 of 28,334 recalls
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...
The Issue: The tracheal tube can kink during patient use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...
The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix L/P with Echo PS 10" X 13" Product Code Recalled by Davol, Inc.,...
The Issue: Product labeling does not match product configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Composix L/P with Echo PS 6" X 8" Product Code Recalled by Davol, Inc.,...
The Issue: Product labeling does not match product configuration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT G3+ Cartridge pH Recalled by Abbott Point Of Care Inc. Due to Abbott...
The Issue: Abbott Point of Care has determined that some individual patient results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Rover Ultra Waste Management System Recalled by Stryker...
The Issue: The purpose of this correction is to upgrade the Neptune 2 Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune 2 Rover Ultra Waste Management System. Recalled by Stryker...
The Issue: The purpose of this correction is to upgrade the Neptune 2 Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Gaymar Medi-Therm device provides a means of regulating patient Recalled...
The Issue: Stryker Medical has identified that on some units of the MTA7900, there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Monitor B650 and CARESCAPE Monitor B850. The...
The Issue: GE Healthcare has recently become aware of potential safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for...
The Issue: A circuit in use was occluded by a blue port cap that was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 7500 Dual Detector System Recalled by Carestream Health,...
The Issue: Carestream Health, Inc. has recalled DR 7500 Dual Detector System utilizing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...
The Issue: Images may be archived to an incorrect or invalid archive location resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...
The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...
The Issue: The locking mechanism that is intended to hold the control panel in a fixed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...
The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...
The Issue: There is a potential for communication loss associated with the F5-01 Frame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System (United States) - Catalys-U: Catalys...
The Issue: Potential for unexpected heating of the transformer mounting bolt located...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.