Besmed Health Business Corporation: Medical Device Recall in 2018 - (Recall #: Z-0109-2019)

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:

Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000

Product Classification:

Class II

Date Initiated: August 9, 2018

Date Posted: October 24, 2018

Recall Number: Z-0109-2019

Event ID: 81009

Reason for Recall:

Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask Sterile

Status: Terminated

Product Quantity: 267 units

Code Information:

Lot Numbers: MO0612G40021 and MO0605G40014

Distribution Pattern:

US Nationwide, and country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated