Medical Device Recall: Z-0019-07

FDA Recalls dataset · Firm: Ciba Vision Corporation · Status: Terminated

Recall Action Class: N/A Date Initiated: 2006-09-13 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0019-07.

Recall Res Number
Z-0019-07
Recalling Firm / Manufacturer
FEI Number
1053053
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2006-09-13
Date Posted
2006-11-04
Date Terminated
2009-02-28
Product Code
LPL
Event Number
36382
Product Quantity
7,132 units
Product Description CSI Flexible Wear, soft (hydrophilic) contact lenses

Reason for Recall Out of specification lens curve

Action Details Consignees were notified via traceable mail on 09/13/2006.

Distribution Pattern Worldwide-U.S., Canada, Australia and Barbados.

Code Information / Serial Numbers Polymer Lot #RM-309824, RM-309691, RM-309631, RM-309592, 03D0201, 03D1401, RM-309825, RM-309762.

Related Establishments / Registrations

Public Record Disclaimer

This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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