# FDA recall Z-2287-2018

> **Teleflex Medical Europe Ltd** · Class II · device recall initiated 2018-06-12.

## Product

Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542    Product Usage:  general surgical scissors

## Reason for recall

The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.

## Distribution

Worldwide Distribution - US Nationwide and the countries of  Canada, India

## Key facts

- **Recall number:** Z-2287-2018
- **Recalling firm:** Teleflex Medical Europe Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-12
- **Report date:** 2018-07-04
- **Termination date:** 2021-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Athlone, Ireland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2287-2018

## Citation

> AI Analytics. FDA recall Z-2287-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2287-2018. Source: US FDA. Licensed CC0.

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