GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. ... recall (Terumo Medical Corporation)
Medical deviceClass IIOngoing
Summary: Terumo Medical Corporation is recalling 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.. Reason: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
What is being recalled
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.
Why
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
Worldwide distribution - US Nationwide and the country of Canada.
How to tell if yours is affected
Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2930-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | June 15, 2026 |
| Reported | August 19, 2026 |
| Company | Terumo Medical Corporation |
| Company location | Elkton, MD, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 7,490 units |
More recalls from Terumo Medical Corporation · all medical device recalls · recalls from June 2026