FDA Class II · Medical device · August 19, 2026
GLIDESHEATH SLENDER A-KIT 6F 10CM recall — Terumo Medical Corporation
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Official ID Z-2930-2026 · Official record ↗
Terumo Medical recalls
Recall found. Terumo Medical is named in FDA Class II recall Z-2930-2026 covering GLIDESHEATH SLENDER A-KIT 6F 10CM. Hazard: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. Identifying details: Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.. Status: Ongoing.
Models with recalls
All Terumo Medical recalls
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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.