Cardiff, United Kingdom
Huntleigh Healthcare Ltd. recalls
1 recall recorded since 2018, most recently on 11 February 2022. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 11 February 2022
- Terminated
- 12 June 2024
- Reason
- Faceplate may become detached from the probe body.
- Distribution
- US Nationwide distribution in the states of OK, CA, GA, MI, VA.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0960-2022
- HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.