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. 2,702 recalls have been distributed to Nevada in the last 12 months.
Showing 4541–4560 of 28,334 recalls
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier I Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint....
The Issue: Failure of adhesive to secure the pole insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier II Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) Recalled by...
The Issue: Complaints have been received that the device inflation tube detached and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviNetics Skull Anchor Key and Drill Kit Recalled by Navinetics Inc Due to...
The Issue: Defective Skull Anchor Key. After attachment of the single use Skull Anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Unit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The firm provided a set of specifications for the device, but some units of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...
The Issue: Calibration Buttons being used in the kitting process were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 1.0 Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altair 330 lbs w/o Hanger Bar Recalled by Human Care Hc Sweden Ab Due to...
The Issue: Patient lift hanger bar may come loose, which could potentially pose risks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE SWABSTICKS PVP 3 PK Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Software Version Numbers version numbers 8B Recalled by RAYSEARCH...
The Issue: A use error that has occurred with RayStation/RayPlan, where material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion manual surgical kits labeled as: a) STERILE 4-1/2" S/S Recalled by...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.