Hill-Rom brand VersaCare Bed; Model P3200.
FDA device recall Z-1482-04 · posted 2004-09-21 · Terminated
Recall details
- Recalling firm
- Hill-Rom, Inc.
- Reason for recall
- Pivot bolts on the sleep deck may become loose and fall out, allowing the head section to shift or to drop to one side, and a grounding warning label is missing.
- Action taken
- Recall letters dated August 24, 2004 were sent to consignees advising them to inspect and monitor the beds until Hill-Rom can visit and make corrections.
- Root cause
- Other
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 5048
- Distribution
- Nationwide, Brazil, Canada, Hong Kong and United Arab Emirates.
- Date initiated
- 2004-08-24
- Date posted
- 2004-09-21
- Date terminated
- 2005-01-31
- Location
- Batesville, IN
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