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 20061–20080 of 28,334 recalls
Recalled Item: ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw Recalled by...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp Recalled...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Periarticular plating system Recalled by Zimmer Manufacturing B.V. Due to A...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaFx Femoral Fixation System Hex head compression screw 4.7 mm Recalled...
The Issue: A small hole may be present in the inner tray of specific lots of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) Recalled by Cordis...
The Issue: Inability to deploy the stent or partial stent deployment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis PRECISE (R) RX Nitinol Stent System (Biliary) Recalled by Cordis...
The Issue: Inability to deploy the stent or partial stent deployment.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...
The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.