Terumo Medical Corporation recalls GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The G
- Recalling company
- Terumo Medical Corporation
- 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.
- Reason
- Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 15, 2026
- Reported
- Aug 19, 2026
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Status
- Ongoing
- Quantity
- 7,490 units
- Lot / codes
- Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.
- Company location
- Elkton, MD
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2930-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2930-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.