Atlas FDA

Vail Enclosed Bed System, model 2000

FDA device recall Z-1026-03 · posted 2003-07-17 · Terminated

Recall details

Recalling firm
Vail Products Inc
Reason for recall
Patients may become entrapped between the bottom side rail and mattress.
Action taken
The firm notified the customers by mail in April 2003, and by telephone, fax, and mail on 6/30/2003.
Root cause
Other
Status
Terminated
Product code
FNL
Quantity affected
891units
Distribution
Nationwide; Canada and Saudi Arabia
Date initiated
2003-04-01
Date posted
2003-07-17
Date terminated
2008-10-29
Location
Toledo, OH

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