Atlas FDA

Hill-Rom brand VersaCare Bed; product P3200.

FDA device recall Z-0402-05 · posted 2005-01-15 · Terminated

Recall details

Recalling firm
Hill-Rom, Inc.
Reason for recall
A potential trip hazard exists when the fracture frame adaptor bracket is installed on the bed without the fracture frame.
Action taken
Customers were notified via letter dated 12/29/04 and informed of the hazard. Hill-Rom will visit each account to place instruction labels on the beds.
Root cause
Other
Status
Terminated
Product code
FNL
Quantity affected
324
Distribution
Nationwide.
Date initiated
2004-12-29
Date posted
2005-01-15
Date terminated
2005-05-09
Location
Batesville, IN

Monitor recalls programmatically

Recalls and clearances share one API, with change alerts when new recalls post.