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Terminated

Magnum II Bariatric Patient Care System

FDA Recall Z-0810-04 · Posted 2004-07-20

Recalling FirmHill-Rom Manufacturing, Inc.
Recall StatusTerminated
Product CodeFNL
Date Initiated2004-03-04
Date Terminated2005-05-24
Product Quantity1424 units

Reason for Recall

Bed may pose a health hazard due to: A) Inability to articulate the frame during transport, B) Exposed sharp edge of footplate, C) Shear point between seat section and lymph panel and D) Patient fall.

Firm Action

Consignees were notified by letter via Federal Express on 3/9/2004.

Root Cause

Other

Distribution Pattern

The Magnum II Bariatric Patient System is primarily leased by hospitals, although some units have been sold Nationwide and Canada.

Official Source

View FDA Recall →

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

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