# FDA recall Z-2533-2020

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2020-05-29.

## Product

RUSCH LASERTUBE (Rubber), RES 102004, Sizes:  a) I.D. mm 4,0, Product Code 102004-000040  b) I.D. mm 5,0, Product Code 102004-000050  c) I.D. mm 6,0, Product Code 102004-000060  d) I.D. mm 7,0, Product Code 102004-000070  e) I.D. mm 8,0, Product Code 102004-000080  Product Usage: Tracheal intubation during laser surgery in the laryngeal area. The tube is resistant to the following kinds of laser: A R+ laser / ND/YAG laser / CO2 lasers (continuous-wave or pulsed) with a wave length ranging from 0.488 ¿m to 10.6 ¿m.

## Reason for recall

Teleflex is initiating a voluntary recall for the above-mentioned products due to reports indicating that the laser guard foil partially separated and/or slightly detached at the edges in the presence of moisture.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2533-2020
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-29
- **Report date:** 2020-07-15
- **Termination date:** 2025-06-17

- **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-2533-2020

## Citation

> AI Analytics. FDA recall Z-2533-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2533-2020. Source: US FDA. Licensed CC0.

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