Atlas FDA

Access Point Medical-Heavy Duty Rollator with Curved Back (rolling walker), Product Code RL12011, with seat, curved back

FDA device recall Z-0155-2007 · posted 2006-11-07 · Terminated

Recall details

Recalling firm
Access Point Medical LLC
Reason for recall
The fork component on the wheel of the Rollator can break due to the use of incorrect manufacturing material and/or molding processes.
Action taken
The recall was initiated by phone on or about 6/20/06, to determine how many Rollators the customer had in stock because they had received reports of Rollators coming out of the box with cracked forks. During the phone call, the customer was told that the recalling firm was bringing back their remaining inventory for inspection and that customer service would be calling them back to arrange for return. The recalling firm issued a '2nd Recall Notice' dated 10/10/06 via UPS between 10/11-13/06 explaining the reason for recall, requesting their customers to conduct a subrecall down to the consumer level and instructing that all of the Rollators be destroyed.
Root cause
Other
Status
Terminated
Product code
ITJ
Quantity affected
Approximately 861 Rollators (total for both models under recalls Z-0154/0155-2007)
Distribution
Nationwide
Date initiated
2006-06-20
Date posted
2006-11-07
Date terminated
2008-06-11
Location
St. Louis, MO

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