Home › FGX INTERNATIONAL INC. › JOE FRESH
JOE FRESH
FGX INTERNATIONAL INC. · Model 10308929.LOB · UDI-DI 00193033447697
10
510(k) clearances
35
Adverse events
1
Recalls
1,111
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-05-02 | Magnivision, Inc. | Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.