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 15221–15240 of 27,884 recalls
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: Binding Site Human IgM Kit (for SPAPLUS) Recalled by The Binding Site Group,...
The Issue: After running the calibration curve, the recovery of the IgM kit control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 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: 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 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: 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: ADVIA Centaur CKMB Calibrator 2-pack Japan 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: 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: 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.
Recalled Item: Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear Recalled by...
The Issue: Johnson and Johnson Vision Care received a number of reports of a partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom EV0-2 with any version of EVOware and EVOware Sample Recalled by...
The Issue: There is a software issue that can potentially impact sample identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ1 Advanced XL Recalled by Qiagen Sciences LLC Due to An issue with the...
The Issue: An issue with the power branching printed circuit board (PCB) on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Polyisoprene Condoms Recalled by Reckitt Benckiser LLC Due...
The Issue: The products failed the filed specification of 1.0kPa for Burst Pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKPS CONTINUOUS EPIDURAL ANES TRAY Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE18TBLS CONT EPIDURAL TRAY Recalled by B. Braun Medical, Inc. Due to The...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTIPLEX TUOHY ULTRA 4 IN CNB400TU Recalled by B. Braun Medical, Inc. Due...
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTI ECHO CT W/2IN TUOHY ULTRA 360 SET Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTIPLEX CONT 4 IN TUOHY ULTRA PNB TRAY Recalled by B. Braun Medical, Inc....
The Issue: The catheter connectors may not stay closed during in and in some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.