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Terminated

Synchron Systems Acetaminophen Reagent, part No. 472169.

FDA Recall Z-1026-04 · Posted 2004-07-20

Recalling FirmBeckman Coulter Inc
Recall StatusTerminated
Product CodeLDP
Date Initiated2003-09-04
Date Terminated2005-01-04
Product Quantityunknown

Reason for Recall

Firm shortened calibration frequency to 7 days from 14 days.

Firm Action

Firm issued letters to customers indicating need to shorten the calibration period from 14 to 7 days.

Root Cause

Other

Distribution Pattern

Nationwide and Canada

Official Source

View FDA Recall →

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

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