Ii - Vi Incorporated: Medical Device Recall in 2018 - (Recall #: Z-1614-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

11-VI Incorporated Laser diode component Non-certified laser diode component used in laser sights for firearms

Product Classification:

Class II

Date Initiated: December 13, 2017

Date Posted: June 13, 2018

Recall Number: Z-1614-2018

Event ID: 80020

Reason for Recall:

Affected diodes incorporated in the laser sights emitted greater than the 5 mW limit.

Status: Terminated

Product Quantity: 323,972

Code Information:

Model Numbers: 25-0655 & 25-0657

Distribution Pattern:

US Distribution to Oregon.

Voluntary or Mandated:

FDA Mandated