STEALTH SPRING CLIP 6mm latis — Class II medical device recall Z-2036-2020
Terminated recall by Applied Medical Resources Corp, reported 2020-05-27, distributed nationwide. Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
| Recall number | Z-2036-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Applied Medical Resources Corp, Rancho Santa Margarita, CA, United States |
| Recall initiated | 2020-01-31 |
| Classified | 2020-05-15 |
| Reported by FDA | 2020-05-27 |
| Terminated | 2022-04-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CH, DE, ES, FI, FR, IT, JP, MX, NL |
| Quantity | 2,240 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00607915110581 |
| Lot numbers | 1357103 |
| Expiration dates | 2024-06-02 |
Product
STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
Reason for recall
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
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-2036-2020. 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.