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Terminated

VAMP Direct Draw, Model VMP700 Needleless cannula for sampling blood.

FDA Recall Z-0242-04 · Posted 2003-12-18

Recalling FirmEdwards Lifesciences AG
Recall StatusTerminated
Product CodeKRA
Date Initiated2003-11-20
Date Terminated2004-11-30
Product Quantity21150

Reason for Recall

Seal integrity, sterility not assured.

Firm Action

Letter was sent to all customers requesting return of the unused lot on 11/20/2003.

Root Cause

Other

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

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

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