# FDA recall Z-0058-2021

> **Medline Industries Inc** · Class II · device recall initiated 2020-09-01.

## Product

ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr  FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.

## Reason for recall

There have been reports of the suction catheter coming apart from the device assembly during use.

## Distribution

62 US consignees; 1 government consignee, 4 foreign consignees

## Key facts

- **Recall number:** Z-0058-2021
- **Recalling firm:** Medline Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-01
- **Report date:** 2020-10-14
- **Termination date:** 2022-05-27

- **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-0058-2021

## Citation

> AI Analytics. FDA recall Z-0058-2021. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0058-2021. Source: US FDA. Licensed CC0.

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