FDA Device recall Z-1852-2022
Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503
- FDA Device
- Class II
- ongoing
- Published 2022-10-05
On 2022-10-05 the FDA classified a Class II recall of Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503 by Surgical Innovations, citing laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1852-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-01-20 |
| Published | 2022-10-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Surgical Innovations |
| Distribution | MA |
Product
Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503; YelloPort Elite Hasson Adaptor 10mm/EA10NH. For use in laparoscopic procedures.
Reason
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
Identifiers
| code_info | Part/UDI-DI/Lot: ET1207503/05051986012438/735479, EA10NH/05051986012100/734029 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1852-2022%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.