Carroll Healthcare brand Arro bed models BA3180-151 AE, BA3180-151 PE, BA3180-151 FE, BA3180-171 AE, BA3180-171 FE and B
FDA device recall Z-0919-05 · posted 2005-06-22 · Terminated
Recall details
- Recalling firm
- Carroll Healthcare Inc.
- Reason for recall
- The diodes in the control panel may fail, which could result in the thermal breakdown of the circuit board inside of the control box, and cause the bed to cease functioning.
- Action taken
- Consignees were sent a fax on 5/17/05 advising them of the problem and instructing them to lock-out the HILO pendant function on the attendant control pad until the firm visits their facility and corrects their beds.
- Root cause
- Other
- Status
- Terminated
- Product code
- FNL
- Distribution
- Nationwide.
- Date initiated
- 2005-05-17
- Date posted
- 2005-06-22
- Date terminated
- 2005-11-17
- Location
- London, Ontario, Canada
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