Atlas FDA

Cidex Plus Test Strips

FDA device recall Z-0375-04 · posted 2004-01-29 · Terminated

Recall details

Recalling firm
Advanced Sterilization Products
Reason for recall
May not accurately detect minimum effective concentration (MEC)
Action taken
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
Status
Terminated
Product code
JOJ
Quantity affected
710 cases, 2 bottles per case
Distribution
Nationwide. Japan, Puerto Rico, Latin America, Caribbean.
Date initiated
2003-12-17
Date posted
2004-01-29
Date terminated
2004-09-10
Location
Irvine, CA

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