Invuity, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2778-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

INVUITY(R) PhotonBlade(TM), REF PB1

Product Classification:

Class II

Date Initiated: June 12, 2017

Date Posted: August 2, 2017

Recall Number: Z-2778-2017

Event ID: 77607

Reason for Recall:

A small number of customer observations were recently received which related to possible unintended energy discharge with the potential to cause tissue damage to patients.

Status: Terminated

Product Quantity: 1328 units

Code Information:

All Lot Numbers

Distribution Pattern:

nationwide

Voluntary or Mandated:

Voluntary: Firm initiated