Abbott Vascular-Cardiac Therapies dba Guidant Corporation Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951
Brand
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Lot Codes / Batch Numbers
Part number 1007848-15, lot number 7052951
Products Sold
Part number 1007848-15, lot number 7052951
Abbott Vascular-Cardiac Therapies dba Guidant Corporation is recalling Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951 due to The affected single lot did not meet an internal specification. One unit failed the test criteria for stent dislodgment testing.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The affected single lot did not meet an internal specification. One unit failed the test criteria for stent dislodgment testing.
Recommended Action
Per FDA guidance
The firm initiated the recall on 07/16/2007 by sending recall letters with attached Customer Reply form via FedEx to each direct account that received the recalled product. Customers were informed of the issue and given instructions to work with their local account representative to review their inventory, remove the recalled product, complete the Customer Reply form and return the recalled product to Abbott Vascular.
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