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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/
Vail Products Inc
235 First St
Toledo OH 43605
For Additional Information Contact
Manufacturer Reason
for Recall
Patients may become entrapped between the bottom side rail and mattress.
FDA Determined
Cause 2
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.