# FDA recall Z-1126-2022

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2022-04-11.

## Product

(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile;  (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile;  (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19061, sterile;  (4) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19062, non-sterile; and   (5) Gibeck Humid-Vent Filter Compact S with Flex Tube, Product #19812, non-sterile.

## Reason for recall

Reports received of torn corrugated breathing tubes.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NV, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI, and WV. The countries of Austria, Australia, Belgium, Canada, Chile, Czech Republic, Finland, France, Germany, Greece, Hong Kong, Hungary, Korea, Malaysia, Netherlands, Panama, Poland, Slovakia, Spain, and Switzerland.

## Key facts

- **Recall number:** Z-1126-2022
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-11
- **Report date:** 2022-06-01

- **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-1126-2022

## Citation

> AI Analytics. FDA recall Z-1126-2022. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1126-2022. Source: US FDA. Licensed CC0.

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