Boston Scientific Corporation: Medical Device Recall in 2018 - (Recall #: Z-0898-2018)

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:

Auriga XL 4007 Laser System, Universal Part Number: M0068FS4007G0. Intended to be used in surgical procedures.

Product Classification:

Class II

Date Initiated: September 22, 2017

Date Posted: March 14, 2018

Recall Number: Z-0898-2018

Event ID: 79096

Reason for Recall:

Certain Auriga consoles have incorrectly assembled trigger wire components. The trigger wire functions in the start-up of the console. An incorrectly assembled trigger wire may result in error codes or failure to start the console.

Status: Terminated

Product Quantity: 9

Code Information:

Serial Number: 20509715, 20465096, 20503137, 20520960, 20541967, 20546219, 20546440, 20575512, and 20575518.

Distribution Pattern:

International Distribution Only -- Australia, Vietnam, France, Germany, Italy, Spain, and Romania.

Voluntary or Mandated:

Voluntary: Firm initiated