# FDA recall Z-1467-2022

> **Covidien Llc** · Class II · device recall initiated 2022-06-07.

## Product

TruClear Hysteroscopic Tissue Removal System Control Unit- designed to meet the requirements of intrauterine tissue removal.    Model Number: 7209808

## Reason for recall

Electrical component failure within the control unit. The observed failure mode is a loss of function of the device when used with handpiece and foot switch.

## Distribution

AZ CA CO IL KS MA MI MN MO NY OK PA TN TX TX WA  Foreign: United Kingdom Ireland Netherlands Reunion Spain

## Key facts

- **Recall number:** Z-1467-2022
- **Recalling firm:** Covidien Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-07
- **Report date:** 2022-08-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mansfield, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1467-2022

## Citation

> AI Analytics. FDA recall Z-1467-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1467-2022. Source: US FDA. Licensed CC0.

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