FDA Medical Device Recalls (openFDA)
Vail Products Inc: Vail Enclosed Bed System, model 2000
- Recall number
- Z-1026-03
- Recalling firm
- Vail Products Inc
- Product
- Vail Enclosed Bed System, model 2000
- Status
- Terminated
- Initiated
- 2003-04-01
- Posted
- 2003-07-17
- Terminated
- 2008-10-29
- Reason
- Patients may become entrapped between the bottom side rail and mattress.
- Root cause
- Other
- Action
- The firm notified the customers by mail in April 2003, and by telephone, fax, and mail on 6/30/2003.
- Quantity
- 891units
- Distribution
- Nationwide; Canada and Saudi Arabia
- Lot, serial or model codes
- All serial numbers affected.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- Firm FEI
- 1000122546
- Firm city
- Toledo
- Firm state
- OH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28