# FDA recall Z-1853-2022

> **Surgical Innovations Ltd** · Class II · device recall initiated 2022-01-20.

## 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.

## Distribution

US: MA

## Key facts

- **Recall number:** Z-1853-2022
- **Recalling firm:** Surgical Innovations Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-20
- **Report date:** 2022-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Leeds, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1853-2022

## Citation

> AI Analytics. FDA recall Z-1853-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1853-2022. Source: US FDA. Licensed CC0.

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