Z-0019-07

CSI Flexible Wear, soft (hydrophilic) contact lenses

Name: Z-0019-07 CSI Flexible Wear, soft (hydrophilic) contact lenses
Creator: Ciba Vision Corporation
Published: 2006-09-13
License: https://open.fda.gov/license/

Alcon Laboratories / initiated 2006-09-13 / Terminated

FDA source

Ciba Vision Corporation began a recall of CSI Flexible Wear, soft (hydrophilic) contact lenses on 2006-09-13. The reason FDA records is "Out of specification lens curve". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0019-07
Status: Terminated
Initiated: 2006-09-13
Posted: 2006-11-04
Terminated: 2009-02-28
Recalling firm: Alcon Laboratories
Product: CSI Flexible Wear, soft (hydrophilic) contact lenses
Product code: LPL Lenses, Soft Contact, Daily Wear
Reason for recall: Out of specification lens curve
FDA root cause: Other
Action: Consignees were notified via traceable mail on 09/13/2006.
Quantity in commerce: 7,132 units
Distribution: Worldwide-U.S., Canada, Australia and Barbados.
Product codes and lots: Polymer Lot #RM-309824, RM-309691, RM-309631, RM-309592, 03D0201, 03D1401, RM-309825, RM-309762.

Product code LPL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)