RegWardenFDA facility compliance records
Recall

Class II — IHB OPERATIONS B.V.

Recalling firmIHB operations
Registered facilityIHB OPERATIONS (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonThe mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.
ProductSkytron Freedom 4FXS-60 Heavy Duty Monitor Mount
Quantity112 units
DistributionUS Nationwide distribution including in the states of AL, AZ, CA, FL, IA, ID, IL, LA, MA, MD, MI, MN, NC, NH, NJ, NM, NY, PA, TN, TX, UT, VA, WI, WV.
Initiated2025-03-27
Classified2025-04-23
Recall numberZ-1663-2025
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — IHB OPERATIONS B.V. (Z-1663-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96581/

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