# FDA recall Z-0941-2022

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2022-03-09.

## Product

Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box

## Reason for recall

The mask cuff may disconnect from the device's breathing tube.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0941-2022
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2022-03-09
- **Report date:** 2022-04-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0941-2022

## Citation

> AI Analytics. FDA recall Z-0941-2022. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-0941-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*