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Terminated

BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.

FDA Recall Z-2378-2018 · Posted None

Recall StatusTerminated
Product CodeOFF
Date Initiated2018-01-12
Date Terminated2020-07-22
Product Quantity6/5-kit cases

Reason for Recall

One of the cases of product might not have been sterilized.

Firm Action

The recalling firm's sales representative telephoned their one customer on 1/12/2018 requesting return of the product.

Root Cause

Process control

Distribution Pattern

The product was distributed to UT.

Official Source

View FDA Recall →

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

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