Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025''
FDA Recall Z-0541-04 · Posted 2004-02-24
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Recalling FirmMagnivision, Inc.
Recall StatusTerminated
Product CodeHQZ
Date Initiated2003-05-02
Date Terminated2012-07-07
Product Quantity145884
Reason for Recall
Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.
Firm 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.
Root Cause
Other
Distribution Pattern
Product was distributed to a a wholesaler in Florida.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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