Vygon U.S.A.: Medical Device Recall in 2019 - (Recall #: Z-1115-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.

Product Classification:

Class II

Date Initiated: December 6, 2018

Date Posted: April 17, 2019

Recall Number: Z-1115-2019

Event ID: 81866

Reason for Recall:

DualStop Caps defect causing leaks in affected product

Status: Terminated

Product Quantity: 107700

Code Information:

Lot codes: 090718FD 250118FD 081117FD 130218FD 050418FD 020518FD

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated