FDA Medical Device Recalls (openFDA)
Ciba Vision Corporation: CSI Toric, soft (hydrophilic) contact lenses
- Recall number
- Z-0020-07
- Recalling firm
- Ciba Vision Corporation
- Product
- CSI Toric, soft (hydrophilic) contact lenses
- Status
- Terminated
- Initiated
- 2006-09-13
- Posted
- 2006-11-04
- Terminated
- 2009-02-28
- Reason
- Out of specification lens curve
- Root cause
- Other
- Action
- Consignees were notified via traceable mail on 09/13/2006.
- Quantity
- 9,740 units
- Distribution
- Worldwide-U.S., Canada, Australia and Barbados.
- Lot, serial or model codes
- Polymer Lot #RM-309824, RM-309691, RM-309631, RM-309592, 03D0201, 03D1401, RM-309825, RM-309762.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LPL
- Firm FEI
- 1053053
- Firm city
- Duluth
- Firm state
- GA
- 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