Vail Products Inc Vail Enclosed Bed System, model 1000 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vail Enclosed Bed System, model 1000
Brand
Vail Products Inc
Lot Codes / Batch Numbers
All serial numbers affected.
Products Sold
All serial numbers affected.
Vail Products Inc is recalling Vail Enclosed Bed System, model 1000 due to Patients may become entrapped between the bottom side rail and mattress.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Patients may become entrapped between the bottom side rail and mattress.
Recommended Action
Per FDA guidance
The firm notified the customers by mail in April 2003, and by telephone, fax, and mail on 6/30/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026