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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