FDA Medical Device Recalls (openFDA)
Vail Products Inc: Vail 2000 Enclosed Bed System.
- Recall number
- Z-0863-05
- Recalling firm
- Vail Products Inc
- Product
- Vail 2000 Enclosed Bed System.
- Status
- Terminated
- Initiated
- 2005-05-06
- Posted
- 2005-06-30
- Terminated
- 2011-01-05
- Reason
- Risk of patient entrapment, may result in serious injury or death.
- Root cause
- Device Design
- Action
- The recalling firm sent consignees an urgent notification letter, dated 5/6/05.
- Quantity
- 1004 beds in distribution.
- Distribution
- Nationwide, Puerto Rico, Canada and Saudi Arabia. MA, RI, NH, ME, VT, CT, NJ, NY, PA, DE, Washington DC, VA, MD, VA, WV, NC, SC, GA, FL, AL, TN, MS, KY, OH, IN, MI, IA, WI, MN, SD, ND, MT, IL, MO, KS, NE, LA, AR, OK, TX, CO, WY, ID, UT, AZ, NM, NV, CA, HI, OR, WA, and AK.
- Lot, serial or model codes
- All serial numbers.
- 510(k) numbers
- ["K963622"]
- 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