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BBIG

BBig B.V. · Model 06147174 · UDI-DI 08719616004181

HQZ
10
510(k) clearances
35
Adverse events
1
Recalls
1,111
Facilities

Description

06147174

Recalls

DateFirmReason
2003-05-02Magnivision, Inc.Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.