Novadaq Technologies Inc.: Medical Device Recall in 2016 - (Recall #: Z-1032-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

PINPOINT Endoscopic Fluorescence Imaging System

Product Classification:

Class II

Date Initiated: January 29, 2016

Date Posted: March 9, 2016

Recall Number: Z-1032-2016

Event ID: 73225

Reason for Recall:

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.

Status: Terminated

Product Quantity: 110 units

Code Information:

Rev. J, Rev. K, Rev. L and Rev. M Model Number : PC9000

Distribution Pattern:

Worldwide Distribution - Nationwide Distribution including Puerto Rico and to the countries of : Bangladesh, Canada, Hong Kong, India, and Israel.

Voluntary or Mandated:

Voluntary: Firm initiated