Recall
FDAHealthJune 15, 2026

Terumo Medical Corporation — GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into

⚠️ Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 15, 2026

Worldwide distribution - US Nationwide and the country of Canada.

What's affected?

Product
GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.
Lot code
0001441871

Additional details

Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 7,490 units.

View original FDA notice →

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