Skip to the content

FDA Medical Device Recalls (openFDA)

Magnivision, Inc.: Product is Magnivision UltraLights reading glasses which have the dioptic power on the label and ''MAGNIVISION AN AMERICAN GREETINGS COMPANY Miramar, FL 33025''

Recall number
Z-0541-04
Recalling firm
Magnivision, 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''
Status
Terminated
Initiated
2003-05-02
Posted
2004-02-24
Terminated
2012-07-07
Reason
Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.
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
145884
Distribution
Product was distributed to a a wholesaler in Florida.
Lot, serial or model codes
Product is not coded.
510(k) numbers
not on file
PMA numbers
not on file
Product code
HQZ
Firm FEI
1000120742
Firm city
Miramar
Firm state
FL
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register