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Terminated

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

FDA Recall Z-1115-2019 · Posted None

Recalling FirmVygon U.S.A.
Recall StatusTerminated
Product CodeFPA
Date Initiated2018-12-06
Date Terminated2020-05-12
Product Quantity107700

Reason for Recall

DualStop Caps defect causing leaks in affected product

Firm Action

Vygon issued recall letter on 12/6/18 via email or fax stating the defect, health risk and action to be taken. Distributors were provided with instructions on how to handle product that was further distributed by them. Contact your local sales representative or Vygons Customer Service Department at 1-800-473-5414, or by e-mail at [email protected]

Root Cause

Equipment maintenance

Distribution Pattern

US Nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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