Gluteraldehyde Concentration Indicators ''Browne GA Indicator for CIDEX PLUS Products''
FDA Recall Z-1479-04 · Posted 2004-09-21
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Recalling FirmAdvanced Sterilization Products
Recall StatusTerminated
Product CodeJOJ
Date Initiated2003-09-04
Date Terminated2005-01-04
Product Quantity11797 cases
Reason for Recall
Performance failure complaints.
Firm Action
Firm issued a Safety Alert to inform users to perform a daily Quality Control check of the test strips to ensure that they are working.
Root Cause
Other
Distribution Pattern
Nationwide, Europe, Latin America, Australia, Canada, and Asia Pacific.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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