GLIDESHEATH SLENDER A-KIT 6F 10CM — Class II medical device recall Z-2930-2026
Ongoing recall by Terumo Medical Corporation, reported 2026-08-19, distributed nationwide. Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
| Recall number | Z-2930-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Terumo Medical Corporation, Elkton, MD, United States |
| Recall initiated | 2026-06-15 |
| Classified | 2026-08-10 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 7,490 units |
| UPC / GTIN / UDI-DI | 00389701011974, 30389701011975 |
| Lot numbers | 0001441871 |
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 for recall
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2930-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.