# FDA recall Z-2922-2020

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2020-08-07.

## Product

Pleur-evac Thoracic Catheters  Catalog No: DTRC-20S    The thoracic catheter is indicated to be used in any surgical procedure requiring attachment to a Chest Drainage device. The thoracic catheter is indicated for use less than 30 days.

## Reason for recall

Potential sterility issue

## Distribution

US Distribution of states to:   AR  AZ  CA  CO  FL  GA  IA  IL  IN  LA  MI  MN  MS  NC  NH  NV  NY  OH  OK  OR  PA  SD  TN  TX  VA  WA  WI

## Key facts

- **Recall number:** Z-2922-2020
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-07
- **Report date:** 2020-09-09
- **Termination date:** 2023-01-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2922-2020

## Citation

> AI Analytics. FDA recall Z-2922-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2922-2020. Source: US FDA. Licensed CC0.

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