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Terminated

Millex-AA Syringe Driven Filter 0.8 um, Sterile Catalog Number: SLAAM33SS

FDA Recall Z-0575-04 · Posted 2004-07-20

Recalling FirmMillipore Corp.
Recall StatusTerminated
Product CodeFPB
Date Initiated2004-01-26
Date Terminated2015-06-11
Product Quantity1 boxes ( 50/box)

Reason for Recall

Lack of assurance of sterility

Firm Action

Millipore notified direct and distributor accounts by Certified letter on 1/26/04. Users are requested to return product. Millipore France and Ireland coordinating recall to the international accounts.

Root Cause

Other

Distribution Pattern

CA, CO, DE, IL, OH, PA, MA, MO, MD, MT, RI, VA Canada

Official Source

View FDA Recall →

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

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