Huntleigh Healthcare Ltd.: Medical Device Recall in 2022 - (Recall #: Z-0960-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 11, 2022

Date Posted: April 27, 2022

Recall Number: Z-0960-2022

Event ID: 89580

Reason for Recall:

Faceplate may become detached from the probe body.

Status: Terminated

Product Quantity: 150 devices

Code Information:

Lot Number: (10) 7842006001 UDI: (01) 05051968036537 (10) 784006001 (individual) UDI: (01) 05051968036544 (10) 784006001 (box)

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated