FDANovember 3, 2021device

OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Malfunction of the automatic laser beam shut-off, the OCT unit might not recognize whether the laser beam is safely switched off

What to do

FDA enforcement status: Ongoing

Brands named

haag streithaaghaag streit

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →