Recall Z-0452-2024— IHB OPERATIONS B.V.
Class II · Ongoing
Class II FDA medical device recall by IHB OPERATIONS B.V., initiated 2023-07-19. FDA's recall record names no specific 510(k) clearance for this event. 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: Weakened connection point on the adjustable suspension arm, potentially causing damage or a break..
- Recalling firm
- IHB OPERATIONS B.V.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-07-19
- Firm location
- Zwolle, Netherlands
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.