Vail 500 Enclosed Bed System.
FDA device recall Z-0861-05 · posted 2005-06-30 · Terminated
Recall details
- Recalling firm
- Vail Products Inc
- Reason for recall
- Risk of patient entrapment, may result in serious injury or death.
- Action taken
- The recalling firm sent consignees an urgent notification letter, dated 5/6/05.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 345 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,
- Date initiated
- 2005-05-06
- Date posted
- 2005-06-30
- Date terminated
- 2011-01-05
- Location
- Toledo, OH
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.