Vygon U.S.A. Recalls

Overview of recall records associated with Vygon U.S.A., including dates, categories and classifications where available.

5recall records

Jun 9, 2021latest record date

May 16, 2018earliest record date

Recall history in this database

Classification mix: Class II: 5.

Medical DeviceJun 9, 2021

Vygon Dressing Change w/ Maxiswab - Product Usage: Custom Dressing Change kit, Product Code recall — FDA Z-1689-2021

Compromised sterile barriers due to the Tyvek Lid not properly adhering to the Tray and has the the potential to cause an infection

Class IIFDA: OngoingVygon U.S.A.

Medical DeviceApr 17, 2019

Vygon DUALSTOP Red Cap used for intravascular lines Product Code: 9888.00 - Product Usage recall — FDA Z-1114-2019

DualStop Caps defect causing leaks in affected product

Class IIFDA: TerminatedVygon U.S.A.

Medical DeviceMay 16, 2018

Vygon U.S.A PICC Tray, Product Code: AMS-9093CP Convenience kit for the insertion of PICCs recall — FDA Z-1637-2018

Potential friction holes may affect the sterility of the product.

Class IIFDA: TerminatedVygon U.S.A.

Medical DeviceMay 16, 2018

Vygon U.S.A PICC Insertion Tray, Product Code: AMS-7192CS-4 Convenience kit for the recall — FDA Z-1640-2018

Potential friction holes may affect the sterility of the product.

Class IIFDA: TerminatedVygon U.S.A.

Medical DeviceMay 16, 2018

Vygon U.S.A Maximum Barrier Insertion Tray, Product Code: AMS-9152CP Convenience kit for the recall — FDA Z-1636-2018

Potential friction holes may affect the sterility of the product.

Class IIFDA: TerminatedVygon U.S.A.

Understanding this recall history

This page summarizes recall records in which the official source identifies Vygon U.S.A. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.