FDA Device recall Z-0970-2024
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
- FDA Device
- Class II
- terminated
- Published 2024-02-07
On 2024-02-07 the FDA classified a Class II recall of Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25 by Vortex Surgical, citing reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilize….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0970-2024 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-12-18 |
| Published | 2024-02-07 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Vortex Surgical |
| Distribution | US |
Product
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25
Reason
Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.
Identifiers
| code_info | UDI/DI 00810123481132, Lot Numbers 2212002 and 2212020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0970-2024%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.