Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,566 recalls have been distributed to Kansas in the last 12 months.
Showing 11941–11960 of 28,538 recalls
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris PCEA Administration Set Recalled by BD SWITZERLAND SARL Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WRIGHT INBONE Tibial Tray Recalled by Wright Medical Technology Inc Due to...
The Issue: One lot of INBONE Tibial Trays is missing the plasma coating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.