Terumo recalls 5 units per box of Glidesheath Slender A-Kit 6F 10CM (Product Code 60-1060) due to incorrect 0.025 guidewire packaging. This may cause catheter placement issues during medical procedures.
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Terumo is recalling 5 units per box of Glidesheath Slender A-Kit 6F 10CM (Product Code 60-1060) because the kit was packaged with a 0.025 guidewire instead of the required 0.021 guidewire. This mismatch could lead to improper catheter placement during medical procedures.
The kit was packaged with a 0.025 guidewire instead of the 0.021 guidewire. This mismatch could lead to improper catheter placement during medical procedures, potentially causing complications.
Medical professionals using the Glidesheath Slender A-Kit for radial artery catheter procedures are most at risk. Patients receiving this procedure may be affected if the incorrect guidewire causes placement issues.
Check for Product Code 60-1060 on the box. The kit contains 5 units per box with a 0.021GW specification but was packaged with 0.025 guidewire.
Look for Product Code 60-1060 on the box to confirm if it's affected.
The Glidesheath Slender A-Kit was packaged with a 0.025 guidewire instead of the required 0.021 guidewire, which could cause improper catheter placement during medical procedures.
5 units per box are affected, with Product Code 60-1060.
The recall record does not specify a remedy, so check the Product Code 60-1060 to confirm if your kit is affected.
We’ve drafted a message you can send Terumo to request your refund or repair — edit it as you like.
Subject: Recall Z-2930-2026 — Terumo Terumo Hello, I own a Terumo that is covered by recall Z-2930-2026 from Terumo. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.