FDA Device Intelligence
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Centerfield 2

OCULUS Optikgeräte Gesellschaft mit beschränkter Haftung · Model 56980 · UDI-DI 04049584000125

HPTHOO
10
510(k) clearances
3
Adverse events
1
Recalls
67
Facilities

Description

Centerfield 2

Recalls

DateFirmReason
2012-08-17Haag-Streit USA IncThe firm recalled the device after learning of a possible deviation in the stimulus luminance of the Perimeter OCTOPUS 101.

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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.