Z-0862-05

Vail 1000 Enclosed Bed System

Name: Z-0862-05 Vail 1000 Enclosed Bed System
Creator: Vail Products Inc
Published: 2005-05-06
License: https://open.fda.gov/license/

Vail Products, Inc. / initiated 2005-05-06 / Terminated / root cause: design

FDA source

Vail Products Inc began a recall of Vail 1000 Enclosed Bed System on 2005-05-06. The reason FDA records is "Risk of patient entrapment, may result in serious injury or death". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-0862-05
Status: Terminated
Initiated: 2005-05-06
Posted: 2005-06-30
Terminated: 2011-01-05
Recalling firm: Vail Products, Inc.
Product: Vail 1000 Enclosed Bed System.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Risk of patient entrapment, may result in serious injury or death.
Root cause tag: design
FDA root cause: Device Design
Action: The recalling firm sent consignees an urgent notification letter, dated 5/6/05.
Quantity in commerce: 3647 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.
Product codes and lots: All serial numbers.

Product code FNL

K982783Class IIVail 1000 Enclosed BedVail Products, Inc. / cleared 1998-10-05

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)