# FDA recall Z-0846-2019

> **Teleflex Medical** · Class II · device recall initiated 2019-01-07.

## Product

Pilling COOLEY SUMP-SUCTION TUBE, REF 351547

## Reason for recall

The internal tip is missing from the device, causing the device to not function as intended.

## Distribution

TX, NY, DC and Philippines

## Key facts

- **Recall number:** Z-0846-2019
- **Recalling firm:** Teleflex Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-07
- **Report date:** 2019-02-27
- **Termination date:** 2021-11-04

- **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-0846-2019

## Citation

> AI Analytics. FDA recall Z-0846-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0846-2019. Source: US FDA. Licensed CC0.

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