Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001 — Class II medical device recall Z-1853-2022
Ongoing recall by Surgical Innovations Ltd, reported 2022-10-05. Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
| Recall number | Z-1853-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Surgical Innovations Ltd, Leeds, N/A, United Kingdom |
| Recall initiated | 2022-01-20 |
| Classified | 2022-09-29 |
| Reported by FDA | 2022-10-05 |
| Quantity | 1 |
| Reason classes | labeling, sterility |
| UPC / GTIN / UDI-DI | 05051986001890 |
Product
Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.
Reason for recall
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
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-1853-2022. 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.