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Robert La Roche

RLR eyewear GesmbH · Model RLRS345RX-04 · UDI-DI 09010491027487

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

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.