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Terminated

Cidex Plus Test Strips

FDA Recall Z-0375-04 · Posted 2004-01-29

Recalling FirmAdvanced Sterilization Products
Recall StatusTerminated
Product CodeJOJ
Date Initiated2003-12-17
Date Terminated2004-09-10
Product Quantity710 cases, 2 bottles per case

Reason for Recall

May not accurately detect minimum effective concentration (MEC)

Firm Action

Recall was made by various emails sent 12/12/2003 to 12/19/2003. Customers are requested to quarantine and return product.

Root Cause

Other

Distribution Pattern

Nationwide. Japan, Puerto Rico, Latin America, Caribbean.

Official Source

View FDA Recall →

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

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