Stryker Trio Mobile Surgery Platform; Model 1033.
FDA device recall Z-1155-06 · posted 2006-06-17 · Terminated
Recall details
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Reason for recall
- An incorrect pin may have been used during assembly and therefore the device may give way during use.
- Action taken
- Consignees were called on 5/15/06 and instructed to discontinue use of these devices until the firm's technician has visited the facility and replaced the pin.
- Root cause
- Other
- Status
- Terminated
- Product code
- FSE
- Quantity affected
- 156
- Distribution
- Worldwide (including USA, Australia, Canada, England, Germany, Italy, Romania and Singapore).
- Date initiated
- 2006-05-15
- Date posted
- 2006-06-17
- Date terminated
- 2006-07-04
- Location
- Portage, MI
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