Guidant Multi-Link Zeta Coronary Stent System
FDA device recall Z-1075-03 · posted 2003-08-01 · Terminated
Recall details
- Recalling firm
- Guidant Corporation ACS
- Reason for recall
- Potential loss of package sterility.
- Action taken
- Firm personnel in China have inspected all Chinese consignee end user inventories. Any units found to be defective have been removed and are currently in Guidant control.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- Not stated
- Distribution
- China
- Date initiated
- 2003-07-15
- Date posted
- 2003-08-01
- Date terminated
- 2004-04-14
- Location
- Temecula, CA
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