Is Terumo Medical Corporation recalled?

Yes — a recall has been published. Reason: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.

TemporaryFDAOngoing

Can cause harm that is usually temporary.

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.

Check the device or its packaging for

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

Why: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Distributed: Worldwide distribution - US Nationwide and the country of Canada.
Company: Terumo Medical Corporation
Announced: 19 August 2026This is the date the recall was announced. A company may have started it weeks earlier.
Recall began: 15 June 2026

Source: FDA record Z-2930-2026 · retrieved 10 August 2026

Every recall is shown word for word from the FDA and USDA, with a link to the source.