FDA Medical Device Recalls (openFDA)
AGFA Corp.: Agfa Cronex 10T Radiographic film
- Recall number
- Z-0471-06
- Recalling firm
- AGFA Corp.
- Product
- Agfa Cronex 10T Radiographic film
- Status
- Terminated
- Initiated
- 2005-12-21
- Posted
- 2006-02-04
- Terminated
- 2006-04-18
- Reason
- Mislabeling; Product labeled Cronex 10T actually contains Afga, Curix Ultra UVL Plus.
- Root cause
- Other
- Action
- Consignees were first contact by telephone followed up with a certified letter, on/about 12/21/2005.
- Quantity
- 118 boxes
- Distribution
- AZ, CA, CO, GA, IL, MI, NE, NV, OH, OR, WA and Canada
- Lot, serial or model codes
- Catalog number LF5D1, Manufacturing Batch or Lot: 79260070
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JAC
- Firm FEI
- 3001236302
- Firm city
- Greenville
- Firm state
- SC
- 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