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.
Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
MedComp is recalling a specific type of medical catheter because it was shipped with the wrong valve size (15F instead of 16F). Using this incorrect valve could lead to complications during medical procedures. This recall affects catheters with the reference number THD155024.
The catheter kits include a 15F valve peelable introducer instead of the required 16F size. This mismatch could cause improper function during medical procedures, potentially leading to complications such as bleeding or infection.
Healthcare professionals using the recalled catheter for medical procedures are most at risk. Patients receiving these catheters during procedures may experience complications due to the incorrect valve size.
Check for the reference number THD155024 on the catheter packaging. The catheter has a 15.SF X 24CM Titan HD size with a 19cm cuff from the tip. Lot numbers starting with MPCT670 and expiration date 12/20/2020 are affected.
Verify the catheter's reference number, lot number, and expiration date to confirm if it matches the recalled items.
The catheter kits were shipped with a 15F valve peelable introducer instead of the correct 16F size, which could cause complications during medical procedures.
The official recall notice does not specify a remedy or action steps for affected users.
Check for the reference number THD155024, lot number starting with MPCT670, and expiration date 12/20/2020 on the packaging.
We’ve drafted a message you can send MedComp to request your refund or repair — edit it as you like.
Subject: Recall Z-2940-2020 — MedComp MedComp Hello, I own a MedComp that is covered by recall Z-2940-2020 from MedComp. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
