FDA Medical Device Recalls (openFDA)
Advanced Sterilization Products: Cidex Plus Test Strips
- Recall number
- Z-0375-04
- Recalling firm
- Advanced Sterilization Products
- Product
- Cidex Plus Test Strips
- Status
- Terminated
- Initiated
- 2003-12-17
- Posted
- 2004-01-29
- Terminated
- 2004-09-10
- Reason
- May not accurately detect minimum effective concentration (MEC)
- Root cause
- Other
- Action
- Recall was made by various emails sent 12/12/2003 to 12/19/2003. Customers are requested to quarantine and return product.
- Quantity
- 710 cases, 2 bottles per case
- Distribution
- Nationwide. Japan, Puerto Rico, Latin America, Caribbean.
- Lot, serial or model codes
- Product code 2924-Lot 010185 Product code 2926-Lot010252
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JOJ
- Firm FEI
- 3003662624
- Firm city
- Irvine
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28