Z-0541-04

Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and...

Name: Z-0541-04 Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and...
Creator: Magnivision, Inc.
Published: 2003-05-02
License: https://open.fda.gov/license/

FGX International Inc. / initiated 2003-05-02 / Terminated

FDA source

Magnivision, Inc. began a recall of Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025'' on 2003-05-02. The reason FDA records is "Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0541-04
Status: Terminated
Initiated: 2003-05-02
Posted: 2004-02-24
Terminated: 2012-07-07
Recalling firm: FGX International Inc.
Product: Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025''
Product code: HQZ Frame, Spectacle
Reason for recall: Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.
FDA root cause: Other
Action: The firm sent an e-mail dated 4/16/03 to their only direct wholesaler telling them to hold the product and followed up with a phone call infomring them of the retagging on 5/2/03 and a sufficient quantify of tags to relabel product at the retail level. Also they visited the wholesaler and retagged in house stock with the smaller tag.
Quantity in commerce: 145884
Distribution: Product was distributed to a a wholesaler in Florida.
Product codes and lots: Product is not coded.

Product code HQZ

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)