FDA recall Z-1008-2026

Beaver-Visitec International, Inc. · Class II · device

Product

BVI Leos Laser and Endoscopy System. Model Number: OME6000U.

Reason for recall

Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The omission of the ferrites on the USB communication cable results in non-conformance to the design specifications, which require two ferrites (one at each end of the cable).

Distribution

US Nationwide distribution in the states of FL, MI, OK, TX, WI.

Key facts

Status
Ongoing
Initiation date
2025-12-05
Report date
2026-01-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Waltham, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1008-2026