YelloPort Elite Universal Seal — Class II medical device recall Z-1396-2022
Completed recall by Surgical Innovations Ltd, reported 2022-07-27, distributed nationwide. There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect
| Recall number | Z-1396-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Surgical Innovations Ltd, Leeds, N/A, United Kingdom |
| Recall initiated | 2022-06-02 |
| Classified | 2022-07-18 |
| Reported by FDA | 2022-07-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CY, CZ, DE, EC, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IT, JO, JP, KW, LB, MX, MY, NO, PL, RU, SA, SE, SG, TH, TR, ZA |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 05051986001562 |
Product
YelloPort Elite Universal Seal. For use in laparoscopic procedures.
Reason for recall
There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect the sterility of the product.
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-1396-2022. 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.