Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,473 recalls have been distributed to West Virginia in the last 12 months.
Showing 15201–15220 of 27,884 recalls
Recalled Item: Capnostream20 (INTL) M Recalled by Oridion Medical 1987 Ltd. Due to The...
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: Capnostream20 M ADULT ICU (CPM) Recalled by Oridion Medical 1987 Ltd. Due to...
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: CAPNOSTREAM 20 (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due to...
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: Capnostream20 (US) M Recalled by Oridion Medical 1987 Ltd. Due to The...
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: 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: Capnostream20 (US)M Recalled by Oridion Medical 1987 Ltd. Due to The...
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: ENDOLOGIX AFX2 Bifurcated Endograft System Recalled by Endologix Due to...
The Issue: Endologix is notifying physicians of patient tailored surveillance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due to...
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: 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: 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: 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: 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 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: 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: 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: 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: 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.