Guidant Corporation ACS Guidant Multi-Link Zeta Coronary Stent System Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Guidant Multi-Link Zeta Coronary Stent System
Brand
Guidant Corporation ACS
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
3050632 3060432 3060251 3051952 3052251 3060331 3051231 3051951 3052752 3052031 3051931 3050651 3052752 3060531 3060451 3050751 3052251 3051951 3050931 3050632 3052032 3060251 3051531 3053051 3051634 3051632 3053051 3051531 3052952 3051552 3050931 3052852 3060431 3060432 3050751 3052131 3051532 3052031 3051631 3050251 3043051 3050931 3051531 3051451 3052851 3051551 3051531 3041031
Guidant Corporation ACS is recalling Guidant Multi-Link Zeta Coronary Stent System due to Potential loss of package sterility.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential loss of package sterility.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026