iBOT 3000 Mobility System, Independence iBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medi
FDA device recall Z-0022-05 · posted 2004-10-19 · Terminated
Recall details
- Recalling firm
- Independence Technology LLC
- Reason for recall
- Rocks and debris can enter into the wheel cluster housing through a damaged wheel cap causing wheel malfunction.
- Action taken
- All individuals/organizations in possession of a device were notified by telephone beginning on August 30, 2004. Letters were mailed to all Customers on 8/31/2004 and to all Clinics on 9/1/2004.
- Root cause
- Other
- Status
- Terminated
- Product code
- IMK
- Quantity affected
- 81 chairs
- Distribution
- The Independence IBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New Zealand. Ten of the US Direct customers received their devices via the VA. One traini
- Date initiated
- 2004-08-30
- Date posted
- 2004-10-19
- Date terminated
- 2005-04-01
- Location
- Warren, NJ
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