FDA Device Intelligence
HomeCliff Weil, Inc. › Red Carpet

Red Carpet

Cliff Weil, Inc. · Model 833 · UDI-DI 00083758408335

HQY
10
510(k) clearances
50
Adverse events
1
Recalls
1,429
Facilities

Description

RED CARPET 833 POLARIZED SUNGLASSES

Recalls

DateFirmReason
2009-11-24LuxotticaThe lenses made for sunglass frames (Liberty Sport Slam or MaxMorpheus) do not meet the lens thickness specification established by the frame manufacturer. The lens thickness rang

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 docs
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.