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U.S. Department of Health and Human Services

Class 2 Device Recall Enclosed Canopy Beds

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  Class 2 Device Recall Enclosed Canopy Beds see related information
Date Initiated by Firm April 01, 2003
Date Posted July 17, 2003
Recall Status1 Terminated 3 on October 29, 2008
Recall Number Z-1026-03
Recall Event ID 26504
Product Classification Bed, Ac-Powered Adjustable Hospital - Product Code FNL
Product Vail Enclosed Bed System, model 2000
Code Information All serial numbers affected.
Recalling Firm/
Manufacturer		 Vail Products Inc
235 First St
Toledo OH 43605
For Additional Information Contact
419-698-3201
Manufacturer Reason
for Recall		 Patients may become entrapped between the bottom side rail and mattress.
FDA Determined
Cause 2		 Other
Action The firm notified the customers by mail in April 2003, and by telephone, fax, and mail on 6/30/2003.
Quantity in Commerce 891units
Distribution Nationwide; Canada and Saudi Arabia
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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