Stryker Secure II hospital bed; model 3002.
FDA device recall Z-0868-03 · posted 2003-06-12 · Terminated
Recall details
- Recalling firm
- Stryker Medical
- Reason for recall
- A wire may break at the crimp and present a potential electric shock hazard.
- Action taken
- The firm sent service representatives to the receiving hospitals, beginning on 5/1/02, and the beds were corrected in place.
- Root cause
- Other
- Status
- Terminated
- Product code
- FNL
- Quantity affected
- 6
- Distribution
- Pennsylvania and Kansas
- Date initiated
- 2003-05-01
- Date posted
- 2003-06-12
- Date terminated
- 2003-06-11
- Location
- Kalamazoo, MI
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