Aerolase Corporation: Medical Device Recall in 2020 - (Recall #: Z-0768-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

LightPod ERA lasers

Product Classification:

Class II

Date Initiated: August 1, 2019

Date Posted: January 15, 2020

Recall Number: Z-0768-2020

Event ID: 84568

Reason for Recall:

This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily available remote interlock connector for the laser device

Status: Terminated

Product Quantity: 65

Code Information:

LightPod ERA Lasers

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated