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Terminated

Vail Enclosed Bed System, model 1000

FDA Recall Z-1025-03 · Posted 2003-07-17

Recalling FirmVail Products Inc
Recall StatusTerminated
Product CodeFNL
Date Initiated2003-04-01
Date Terminated2008-10-29
Product Quantity1,008 units

Reason for Recall

Patients may become entrapped between the bottom side rail and mattress.

Firm Action

The firm notified the customers by mail in April 2003, and by telephone, fax, and mail on 6/30/2003.

Root Cause

Other

Distribution Pattern

Nationwide; Canada and Saudi Arabia

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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