Stryker Epic Critical Care Bed; Model 2030.
FDA device recall Z-0554-06 · posted 2006-03-31 · Terminated
Recall details
- Recalling firm
- Stryker Medical
- Reason for recall
- The bed exit may not alarm as appropriate.
- Action taken
- The firm began visiting accounts to install new software on 1/17/06 and expects completion of installation at all accounts by 3/31/06.
- Root cause
- Other
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 68
- Distribution
- World Wide--(Chile, Mexico and Singapore)
- Date initiated
- 2006-01-17
- Date posted
- 2006-03-31
- Date terminated
- 2006-07-03
- Location
- Kalamazoo, MI
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