Magseed Pro 7 cm soft tissue marker — Class II medical device recall Z-0316-2026
Ongoing recall by ENDOMAGNETICS LTD, reported 2025-11-05, distributed nationwide. Potential for contamination with cotton fibers.
| Recall number | Z-0316-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ENDOMAGNETICS LTD, Cambridge, N/A, United Kingdom |
| Recall initiated | 2025-10-01 |
| Classified | 2025-10-24 |
| Reported by FDA | 2025-11-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,760 units |
| UPC / GTIN / UDI-DI | 15060391210459 |
| Lot numbers | 241227-01, 250212-02, 250324-03, 250415-06, 250523-11, 250612-51 |
| Model numbers | MS2-17-1-07 |
Product
Magseed Pro 7 cm soft tissue marker. Model Number: MS2-17-1-07. Product Description: The Endomag Magseed Pro Magnetic Marker System is a sterile, single use device composed of a marker preloaded in a 17ga Needle Delivery System. The Endomag Magseed Pro Marker is indicated for use to radiographically mark soft tissue during a surgical procedure or for future surgical procedures.
Reason for recall
Potential for contamination with cotton fibers.
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-0316-2026. 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.