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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