Every recall we track for Medical Components, Inc dba MedComp — 29 in all — plus the complaints and injury reports the public filed about them.
MedComp recalls Power Injectable CT Port insertion kits with incorrect 6.6F port instead of 5F. This may cause prolonged surgery and increased surgical risks. Affected kits have catalog number MRDP50AXS.
MedComp recalls 15.SF X 24CM Titan HD catheters with incorrect 15F valve instead of 16F. This mismatch may cause complications during medical procedures. Affected units have specific lot numbers and expiration dates.
MedComp recalls 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits (Item MC061425) due to containing non-valved introducers instead of valved ones. This could lead to complications during dialysis procedures.
MedComp recalls 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits with a non-valved introducer instead of valved. This could lead to complications during dialysis procedures.
MedComp recalls 14F x 24CM SLX Double Lumen Hemodialysis catheter kits that contain a non-valved introducer instead of the labeled valved type. This could lead to complications during dialysis procedures.
MedComp recalls 14F SLX Double Lumen Hemodialysis catheter kits that contain non-valved introducers instead of valved ones, which could cause complications during dialysis.
MedComp recalls C3 Wave App v. 2.0.5 due to ECG waves not appearing after iOS 12 update, risking incorrect PICC placement.
MedComp recalls Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Sets due to risk of suture wings cracking, which could cause catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls DUO FLOW Custom Trays with serial numbers 414, 415, and 67 due to risk of suture wings cracking, which could cause catheter dislocation, bleeding, or air emboli. Six complaints reported without serious injury.
MedComp recalls Duo-Flow XTP Straight Full Sets (RMS02105, RMS02108) due to risk of suture wings cracking, which could cause catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls DUO FLOW double lumen catheters with potential suture wing cracks leading to catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls Duo-Flow IJ Full Tray models with potential suture wing cracks causing catheter dislocation, bleeding, or air emboli. Six complaints reported without serious injury.
MedComp recalls specific double lumen catheter sets due to potential suture wing cracking, which may cause catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls SOFT-LINE DUO-FLOW double lumen catheter trays (T3500, T4000, T4400, T4424) due to risk of suture wings cracking, which could cause catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls Duo-Flow Double Lumen Catheters with potential suture wing cracks leading to dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls Duo-Flow Catheter Full Tray kits for potential suture wing cracks causing catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls Duo-Flow XTP Straight Full Sets and hemodialysis catheter insertion kits (AAC02106-02108) due to potential suture wing cracks causing catheter dislocation, bleeding, or air emboli. Six complaints reported with no serious injuries.
MedComp recalls SOFT-LINE DUO-FLOW double lumen catheter sets (T94C, T9: 150 characters
MedComp recalls 12F Tesio Catheter Set (MCTC1235SM) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedComp recalls repair kit ARA101 (UDI 884908083637) due to potential connection failures causing blood loss or air emboli. Affected users should contact MedComp for details.
MedComp recalls catheter repair kit AAC52001 with UDI 884908001891 due to potential connection failures causing blood loss or air emboli. Affected units include specific lot numbers.
MedComp recalls TWO PART ADAPTER REF MCTLA2000 due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedComp recalls catheter repair kit RMS52001 with UDI 884908039658 due to potential connection failures causing blood loss or air emboli. Affected units include specific lot numbers.
MedComp recalls repair kit RPK-01 with UDI 884908039856 due to potential blood loss or air emboli from connection failures in hemodialysis tubing.
MedComp recalls 12F Tesio Catheter Sets with specific lot numbers due to potential connection failures that could cause blood loss or air emboli. Affected units include MCTC1235SD model with UDI 884908027242.
MedComp recalls 12F X 60CM TESIO Catheter Sets with Y Adapter (REF CMD757) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedComp recalls 12F X 40CM TESIO Catheter Sets with Y-adapter (ref CMD755) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers.
MedComp recalls 12F Tesio Catheter Set (REF MCTC1247SD) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedComp recalls 8F Plastic Dignity Low Profile CT Port kits with incorrect unmarked guidewires. These kits may cause complications during medical procedures. Affected kits have specific lot numbers and expiration dates.
