# FDA recall Z-0960-2022

> **Huntleigh Healthcare Ltd.** · Class II · device recall initiated 2022-02-11.

## Product

HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8

## Reason for recall

Faceplate may become detached from the probe body.

## Distribution

US Nationwide distribution in the states of OK, CA, GA, MI, VA.

## Key facts

- **Recall number:** Z-0960-2022
- **Recalling firm:** Huntleigh Healthcare Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-11
- **Report date:** 2022-04-27
- **Termination date:** 2024-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cardiff, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0960-2022

## Citation

> AI Analytics. FDA recall Z-0960-2022. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0960-2022. Source: US FDA. Licensed CC0.

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