Data Foundry

Medical device recalls 2023

Freedom Boom models series: F110 — Class II medical device recall Z-0452-2024

Ongoing recall by IHB OPERATIONS B.V., reported 2023-12-13, distributed in AL, AR, AZ, CA, CO, CT, FL, GA…. Weakened connection point on the adjustable suspension arm, potentially causing damage or a break.

Recall numberZ-0452-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmIHB OPERATIONS B.V., Zwolle, Netherlands
Recall initiated2023-07-19
Classified2023-12-01
Reported by FDA2023-12-13
DistributedAL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, LA, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OH, OK, PA, TN, TX, UT, VA, VT, WA, WI, WV
Quantity1,497
Reason classesdevice malfunction
UPC / GTIN / UDI-DI10841736115951, 10841736115968, 10841736115975, 10841736116491, 10841736116545, 10841736116576, 10841736116590, 10841736116651
Model numbers42A-43H, 42A-43L, 42A-43M, 42A-43S

Product

Freedom 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.

Reason for recall

Weakened connection point on the adjustable suspension arm, potentially causing damage or a break.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0452-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.