Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.
FDA device recall Z-0206-04 · posted 2003-12-10 · Terminated
Recall details
- Recalling firm
- Hill-Rom, Inc.
- Reason for recall
- The ambulatory assist bar may not lock into position and may come out of place due to incorrect assembly.
- Action taken
- Customers were advised of the recall by letter dated 11/12/03 and mailed on 11/14/03. A Hill-Rom representative will visit each customer to assure the latching mechanism is properly attached to the bed.
- Root cause
- Other
- Status
- Terminated
- Product code
- KMM
- Quantity affected
- 1400
- Distribution
- United States and Canada
- Date initiated
- 2003-11-14
- Date posted
- 2003-12-10
- Date terminated
- 2004-08-06
- Location
- Batesville, IN
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