Class II

Medical Device Recall: 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.

Terumo Medical Corporation · June 15, 2026

Reason for Recall

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

Distribution

Worldwide distribution - US Nationwide and the country of Canada.

States Affected

NATIONWIDE

Quantity Affected

7,490 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2930-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.