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
ReasonWeakened connection point on the adjustable suspension arm, potentially causing damage or a break.
ProductFreedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm part numbers 42A-43L, 42A-43M, 42A-43H, and 42A-43S. Ceiling mounted utilities and equipment dispensing system.
Quantity1,497
DistributionUS: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MB, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OH, OK, PA, TN, TX, UT, VA, VT, WA, WI, WV.
Initiated2023-07-19
Classified2023-12-01
Recall numberZ-0452-2024
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-0452-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93351/

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