Z-0400-03

Cosmetic color soft contact lenses. Multiple colors which include Blue, Green, Aqua, Brown, Grey. BesCon...

Name: Z-0400-03 Cosmetic color soft contact lenses. Multiple colors which include Blue, Green, Aqua, Brown, Grey. BesCon...
Creator: My Cosmetics Inc
Published: 2002-11-13
License: https://open.fda.gov/license/

My Cosmetics Inc / initiated 2002-11-13 / Terminated / root cause: labeling and UDI

FDA source

My Cosmetics Inc began a recall of Cosmetic color soft contact lenses. Multiple colors which include Blue, Green, Aqua, Brown, Grey. BesCon (brand) on 2002-11-13. The reason FDA records is "Products are being distributed from importer directly to retail outlets labeled 'for cosmetic use only'". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as labeling and UDI.

Recall record

Recall number: Z-0400-03
Status: Terminated
Initiated: 2002-11-13
Posted: 2002-12-31
Terminated: 2005-01-04
Recalling firm: My Cosmetics Inc
Product: Cosmetic color soft contact lenses. Multiple colors which include Blue, Green, Aqua, Brown, Grey. BesCon (brand)
Product code: LPL Lenses, Soft Contact, Daily Wear
Reason for recall: Products are being distributed from importer directly to retail outlets labeled 'for cosmetic use only'
Root cause tag: labeling and UDI
FDA root cause: Other
Action: Firm began to telephone contact recall customers on 11/20/2002. Letters will also be sent requesting return of any remaining stock.
Distribution: Nationwide. States of AL, AR, CA, DE, FL, GA, KY, LA, MD, MS, MO, NV, NY, NC, NE, OK, TN, TX, WA.
Product codes and lots: Lot numbers BB63 and BB73 on containers that hold lenses. Lot number 123410 is on inner box that holds 3 pairs of lenses.

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)