Surgical Table Column Casing Revision B, Product #0788-200-001 Revision B; component of Stryker's VERTIER Surgical Table
FDA device recall Z-2189-2008 · posted 2008-09-17 · Terminated
Recall details
- Recalling firm
- Stryker Communications Corp
- Reason for recall
- Potential exists for energy chain, which is responsible for protecting hydraulic and electrical cables during up and down motion on VERTIER Surgical Table, to become lodged between column case sections resulting in possible reduction or lose of function to hand and/or foot controls or possible involuntary movement of the table.
- Action taken
- Firm notified consignees via letter titled URGENT: Device Recall, dated 04/01/08. Consignees notified of issue and were told a company representative would visit the firm to perform the required maintenance. Contact Karen Smith-Mosley at 972-410-7310 if you have questions.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FQO
- Quantity affected
- 10 units.
- Distribution
- Nationwide distribution to the following states: CA, CO, TX and UT.
- Date initiated
- 2008-05-01
- Date posted
- 2008-09-17
- Date terminated
- 2010-01-08
- Location
- Flower Mound, TX
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