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Terminated

Hill-Rom brand VersaCare Bed; Model P3200.

FDA Recall Z-1482-04 · Posted 2004-09-21

Recalling FirmHill-Rom, Inc.
Recall StatusTerminated
Product CodeFNL
Date Initiated2004-08-24
Date Terminated2005-01-31
Product Quantity5048

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.

Firm Action

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

Distribution Pattern

Nationwide, Brazil, Canada, Hong Kong and United Arab Emirates.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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