# FDA recall Z-2749-2020

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2020-06-30.

## Product

Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish and maintain normal intra-thoracic pressure gradients. To facilitate complete lung re-expansion to restore normal breathing dynamics.

## Reason for recall

Potential for sterile packaging to be compromised¿

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of FL, PR and the countries of AL, BR, CR, EC, ES, GB, GR, HK, HN, ID, IT, MX, PA, PE, PH, PK, PR, SG, SV, VE.

## Key facts

- **Recall number:** Z-2749-2020
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-06-30
- **Report date:** 2020-08-12

- **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-2749-2020

## Citation

> AI Analytics. FDA recall Z-2749-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2749-2020. Source: US FDA. Licensed CC0.

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