Latest recalls
FDAClass IIAugust 19, 2026

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…

Why it was recalled

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

What to do

The recall is ongoing. Follow the firm and FDA instructions.

Affected products and identifiers

Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871. — 7,490 units

Record details

Terumo Medical Corporation — Worldwide distribution - US Nationwide and the country of Canada.

Open FDA enforcement record