HUNTLEIGH Disposable intraoperative Probe — Class II medical device recall Z-0960-2022
Terminated recall by Huntleigh Healthcare Ltd., reported 2022-04-27, distributed nationwide. Faceplate may become detached from the probe body.
| Recall number | Z-0960-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Huntleigh Healthcare Ltd., Cardiff, United Kingdom |
| Recall initiated | 2022-02-11 |
| Classified | 2022-04-20 |
| Reported by FDA | 2022-04-27 |
| Terminated | 2024-06-12 |
| Distributed | Nationwide (US) |
| Quantity | 150 devices |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 05051968036537, 05051968036544 |
| Lot numbers | 784006001, 7842006001 |
| Model numbers | DIOP8, DIPP10 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0960-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.