Guidant Corporation ACS Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numbers have been listed. The firm indicates that total numbers of devices subject to this removal are being defined. Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numbers have been listed. The firm indicates that total numbers of devices subject to this removal are being defined.
Brand
Guidant Corporation ACS
Lot Codes / Batch Numbers
All lots are included in the action.
Products Sold
All lots are included in the action.
Guidant Corporation ACS is recalling Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numbers have due to Complaints that the stents are being dislodged from the delivery system.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Complaints that the stents are being dislodged from the delivery system.
Recommended Action
Per FDA guidance
Information as an Advisory Notice was sent by facsimile to the Competent Authorities and to distributors on April 1 2003. Recall letters will be delivered by hand in most instances.
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