Vygon Corporation Premicath 28G PICC Catheter Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Premicath 28G PICC Catheter
Brand
Vygon Corporation
Lot Codes / Batch Numbers
Lot numbers 014434 and 012615
Products Sold
Lot numbers 014434 and 012615
Vygon Corporation is recalling Premicath 28G PICC Catheter due to Guidewire protuding from tip of the catheter. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Guidewire protuding from tip of the catheter
Recommended Action
Per FDA guidance
The recalling firm issued a recall letter via fax to the distributors on 6/27/05. The letter informed the distributors of the problem and to notify any hospital accounts of the problem and the need to trim the catheter prior to implantation.
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 noticeDistribution
As reported by FDA
CA, CO, FL, IL, IN, MD, NJ, NY, OH, PA, TX, WA
Page updated: Jan 10, 2026