Clarus Medical, Llc: Medical Device Recall in 2021 - (Recall #: Z-2405-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

Product Classification:

Class II

Date Initiated: July 27, 2021

Date Posted: September 8, 2021

Recall Number: Z-2405-2021

Event ID: 88399

Reason for Recall:

The sterile barrier seal may be compromised.

Status: Terminated

Product Quantity: 858 units

Code Information:

Model Numbers 1100-002 and 1100-002 SHORT; Serial Numbers 64139 through 65022

Distribution Pattern:

Distribution in US - 18 accounts 1 foreign account

Voluntary or Mandated:

Voluntary: Firm initiated