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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

IHB OPERATIONS B.V.: Freedom Boom Suspension Arms Recalled for Structural Break Risk

Agency Publication Date: December 1, 2023
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Summary

IHB OPERATIONS B.V. has recalled 1,497 Freedom Boom ceiling-mounted utility systems including models F110, F120, F130, F320, F330, F350, F410, and F420. These systems, used in medical settings to dispense utilities and support equipment, contain a weakened connection point on the adjustable suspension arm. This defect can cause the arm to damage or break during use, potentially leading to falling equipment. Consumers should identify if their units contain the specific 42A Lightweight Spring Arm components and contact the manufacturer for a solution.

Risk

The connection point on the adjustable suspension arm is weakened and may fail. If the arm breaks, the attached medical equipment or utility dispensers could fall unexpectedly, posing a risk of impact injuries to patients or healthcare providers and causing critical equipment failure.

What You Should Do

  1. Identify if your facility uses Freedom Boom model series F110, F120, F130, F320, F330, F350, F410, or F420.
  2. Check the specific part numbers for the built-in 42A Lightweight Spring Arm; affected parts include 42A-43L, 42A-43M, 42A-43H, and 42A-43S.
  3. Verify the UDI-DI on your equipment: 10841736115951 (F110), 10841736115968 (F120), 10841736115975 (F130), 10841736116491 (F320), 10841736116545 (F330), 10841736116576 (F350), 10841736116590 (F410), or 10841736116651 (F420).
  4. Contact your healthcare provider, facility manager, or IHB OPERATIONS B.V. at their Zwolle, Netherlands headquarters for further instructions regarding the repair or replacement of the weakened suspension arms.
  5. For additional questions, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Contact the manufacturer regarding the weakened suspension arm defect.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Freedom Boom F110 SERIES Ceiling Mounted Utility System
Model / REF:
F110
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736115951
Product: Freedom Boom F120 SERIES Ceiling Mounted Utility System
Model / REF:
F120
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736115968
Product: Freedom Boom F130 SERIES Ceiling Mounted Utility System
Model / REF:
F130
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736115975
Product: Freedom Boom F320 SERIES Ceiling Mounted Utility System
Model / REF:
F320
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736116491
Product: Freedom Boom F330 SERIES Ceiling Mounted Utility System
Model / REF:
F330
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736116545
Product: Freedom Boom F350 SERIES Ceiling Mounted Utility System
Model / REF:
F350
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736116576
Product: Freedom Boom F410 SERIES Ceiling Mounted Utility System
Model / REF:
F410
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736116590
Product: Freedom Boom F420 SERIES Ceiling Mounted Utility System
Model / REF:
F420
42A-43L
42A-43M
42A-43H
42A-43S
Lot Numbers:
UDI-DI: 10841736116651

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93351
Status: Active
Manufacturer: IHB OPERATIONS B.V.
Sold By: authorized medical equipment distributors
Manufactured In: Netherlands
Units Affected: 1,497
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.