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. 2,526 recalls have been distributed to Wyoming in the last 12 months.
Showing 11721–11740 of 27,462 recalls
Recalled Item: therascreen EGFR RGQ PCR Kit (24) Recalled by Qiagen Sciences LLC Due to...
The Issue: There is a risk for a false mutation positive result in rare cases resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAC Tray/5 Catheter Introducer Tray 8F Recalled by Argon Medical Devices,...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Line Kit 20ga X 3" Recalled by Argon Medical Devices, Inc Due to...
The Issue: Arterial Line Kits include thicker curved reverse-cutting needle with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 Automation System using the Aliquoter Module (Inpeco P/N...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: In certain firmware versions, in case a Clot Detection error (error code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Augomation System using the Aliquoter Module (Inpeco P/N FLX-212)...
The Issue: Potential for discrepant patient results due to a potential for the primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation System with Advia2120LAS Interface Module (P/N FLX-219-00...
The Issue: The identified problem is an erroneous association between the carrier and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oryx Cervical Screw Caddy Recalled by Innovasis, Inc Due to Cervical screw...
The Issue: Cervical screw caddies have incorrect text markings for the 4.5mm Fixed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inpeco FlexLab Recalled by Inpeco S.A. Due to When analyzer sample carousel...
The Issue: When analyzer sample carousel lid remains open or manual process is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Accelerator a3600 Recalled by Inpeco S.A. Due to When analyzer sample...
The Issue: When analyzer sample carousel lid remains open or manual process is too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Recalled by...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemashield Gold Knitted Microvel Double Velour Vascular Graft...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch...
The Issue: Potential small holes at the seam lines of Hemashield branches causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.