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Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to
Recalled August 19, 2026 · FDA recall Z-2930-2026 · Terumo Medical
Hazard
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire. · FDA Class II
Units
7,490 units
Sold at
Worldwide distribution - US Nationwide and the country of Canada.
Description
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
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.
Manufacturer(s)
Terumo Medical Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →