# FDA recall Z-1683-2022

> **Medline Industries Inc.** · Class II · device recall initiated 2022-07-21.

## Product

Medline CHEST TUBE REORDER NO: DYNJ36762A

## Reason for recall

Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit

## Distribution

U.S. Nationwide distribution in the state of AL.

## Key facts

- **Recall number:** Z-1683-2022
- **Recalling firm:** Medline Industries Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-21
- **Report date:** 2022-09-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Laredo, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1683-2022

## Citation

> AI Analytics. FDA recall Z-1683-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1683-2022. Source: US FDA. Licensed CC0.

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