# FDA recall Z-0108-2023

> **Medicina Uk Ltd** · Class II · device recall initiated 2022-07-04.

## Product

Medicina ENFit 5ml Reusable Enteral Syringe    Code: LHE05

## Reason for recall

Plunger component has been manufactured with an unapproved material (Polyethylene not Polypropylene) and does not meet raw material specification

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-0108-2023
- **Recalling firm:** Medicina Uk Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-04
- **Report date:** 2022-10-26

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0108-2023

## Citation

> AI Analytics. FDA recall Z-0108-2023. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-0108-2023. Source: US FDA. Licensed CC0.

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