FDA Device recall Z-2035-2020
STEALTH SPRING CLIP 6mm latis (1/4 Force)
- FDA Device
- Class II
- terminated
- Published 2020-05-27
On 2020-05-27 the FDA classified a Class II recall of STEALTH SPRING CLIP 6mm latis (1/4 Force) by Applied Medical Resources, citing failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2035-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-01-31 |
| Published | 2020-05-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Applied Medical Resources |
| Distribution | US |
Product
STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.
Reason
Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Identifiers
| code_info | LOT # 1360356, Manufacture Date July 5, 2019; Expiration Date July 3, 2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2035-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.