Atlas FDA

Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm

FDA device recall Z-0452-2024 · posted 2023-12-01 · Open, Classified

Recall details

Recalling firm
IHB OPERATIONS B.V.
Reason for recall
Weakened connection point on the adjustable suspension arm, potentially causing damage or a break.
Action taken
A recall notification issued October 09, 2023 via certified mail . Follow-up will be made by service representatives within 2 weeks to arrange for correction to replace all bearing assemblies in the field with an updated design. Prior to the field correction, inspect your Freedom 42A Lightweight Spring Arm for any movement in the end bearing assembly. If any loose connections are identified, please immediately remove the Spring Arm from use and notify your local authorized representative. Address questions or concerns to your local authorized representative or Skytron at 1-800-759-8766.
Root cause
Device Design
Status
Open, Classified
Product code
FQO
Quantity affected
1,497
Distribution
US: 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.
Date initiated
2023-07-19
Date posted
2023-12-01
Location
Zwolle, Netherlands

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