FDA Recall Open, Classified

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

Recall: Z-1008-2026 · Initiated December 5, 2025

Recall

Recall Number
Z-1008-2026
Event Number
98076
Firm
Beaver-Visitec International, Inc.
FEI Number
1211998
Product Code
HQF
Status
Open, Classified
Root Cause
Process control
Initiated
December 5, 2025
Posted
December 31, 2025
Address
500 Totten Pond Rd, Waltham, MA, 02451-1916

Description

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

Reason

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).

Action

Beaver-Visitec International (BVI) notified consignees via emailed letter on 12/05/2025. Consignees were informed that the affected units can still be used. A BVI service technician will contact each consignee to schedule a visit. During this visit, the missing ferrites will be installed to restore the equipment to its fully compliant and validated configuration. BVI aims to complete the correction by December 31st, 2025.

Distribution

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

Quantity

5 units