Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14961–14980 of 27,462 recalls
Recalled Item: CAPNOSTREAM 20P (INTL) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 900 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Complaints received of sporadic erroneously elevated platelet results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Complaints received of sporadic erroneously elevated platelet results...
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: Complaints received of sporadic erroneously elevated platelet results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system...
The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality¿ Spinal Fixation System.Spinal Intervertebral Body Recalled by...
The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality¿ Spinal Fixation System. Spinal Interlaminal Recalled by Zimmer...
The Issue: The Vitality Shear-off Set Screw is not threading properly with the mating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Interventional Fluoroscopic X-Ray System Recalled by Siemens Medical...
The Issue: Temperature of the detector may fall out of its designed working range (cool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: Temperature of the detector may fall out of its designed working range (cool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XN-Series Fluorocell PLT Recalled by Sysmex America, Inc. Due to The...
The Issue: The fluorescent platelet counts (PLT-F) and immature platelet fraction (IPF)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers...
The Issue: Affected lots of reprocessed arthroscopic shavers may display the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO V-PRO 1 Recalled by Steris Corporation Due to There is the potential...
The Issue: There is the potential for a scenario where a punctured cup of sterilant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Li-ion battery packs used in BIS Vista and BIS View Recalled by Covidien LLC...
The Issue: Revised replacement instructions for the Li-ion battery packs used in BIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: Recalled...
The Issue: When creating a correction plan with the Correct Axial First button selected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CKMB Calibrator Recalled by Siemens Healthcare Diagnostics,...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE...
The Issue: BioFlo Ports was partially manufactured with the incorrect sterile port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Recalled by Diagnostica Stago, Inc....
The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CKMB Calibrator Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CKMB Master Curve Material Recalled by Siemens Healthcare...
The Issue: A potential bias was identified with certain kits compared to the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostica Stago STA N¿oplastine¿ CI Plus Recalled by Diagnostica Stago,...
The Issue: QC values outside of the assigned ranges (prolonged Prothrombin time /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.