# FDA recall Z-0083-2018

> **Teleflex Medical** · Class II · device recall initiated 2017-10-05.

## Product

WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO

## Reason for recall

The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.

## Distribution

Nationwide and Australia, Canada, Singapore, Thailand, China, Taiwan, Belgium, Japan, S. Korea

## Key facts

- **Recall number:** Z-0083-2018
- **Recalling firm:** Teleflex Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-05
- **Report date:** 2017-11-15
- **Termination date:** 2023-01-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Research Triangle Park, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0083-2018

## Citation

> AI Analytics. FDA recall Z-0083-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0083-2018. Source: US FDA. Licensed CC0.

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