AllClear
PricingSign in
FDAJanuary 29, 2016device

PINPOINT Endoscopic Fluorescence Imaging System

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

The hazard

It has been determined that the PINPOINT Operator's Manual does not contain validated parameters for gravity-cycle autoclave sterilization of the PINPOINT laparoscopes and light guide cable in the reprocessing tray.

What to do

FDA enforcement status: Terminated

Brands named

novadaq technologiesnovadaq

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 →