Atlas FDA

Magnum II Bariatric Patient Care System

FDA device recall Z-0810-04 · posted 2004-07-20 · Terminated

Recall details

Recalling firm
Hill-Rom Manufacturing, Inc.
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.
Action taken
Consignees were notified by letter via Federal Express on 3/9/2004.
Root cause
Other
Status
Terminated
Product code
FNL
Quantity affected
1424 units
Distribution
The Magnum II Bariatric Patient System is primarily leased by hospitals, although some units have been sold Nationwide and Canada.
Date initiated
2004-03-04
Date posted
2004-07-20
Date terminated
2005-05-24
Location
Charleston, SC

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