Atlas FDA

Bari Maxx II, KCI''s BariMaxx II bariatric bed, P/N 310611, November 2001, KCI The Clinical Advantage, P. O. Box 659508,

FDA device recall Z-0129-06 · posted 2005-11-08 · Terminated

Recall details

Recalling firm
Kinetic Concepts, Inc
Reason for recall
Design change to uppgrade reliability of powered adjustable bed.
Action taken
All consignees were notified with a technical bulletin explaining the inspection and addition of washers to the set-screws.
Root cause
Other
Status
Terminated
Product code
FNL
Quantity affected
93 beds
Distribution
Nationwide
Date initiated
2004-08-16
Date posted
2005-11-08
Date terminated
2005-11-08
Location
San Antonio, TX

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