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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