FDA Recall Terminated

Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000

Recall: Z-0109-2019 · Initiated August 9, 2018

Recall

Recall Number
Z-0109-2019
Event Number
81009
Firm
Besmed Health Business Corporation No.5, Lane 116, Wu-Kong 2nd Road Wu-Ku District New Taipei City Taiwan
FEI Number
3003256355
Product Code
CAE
Status
Terminated
Root Cause
Error in labeling
Initiated
August 9, 2018
Terminated
May 10, 2019

Description

Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000

Reason

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

Action

Ambu issued via USPS Certified Mail/Email to customers on Aug 09, 2018 advising users of the problem. If you have affected lot in stock and you are using it as Reusable Laryngeal Mask (following accompanying instruction for use), you can continue to use it and no need to return it. Accounts requested to see if you have affected lots in stock. If you do have it, check Aura40 Standard devices for incorrect labelled pouch, and place wrongly labelled products in quarantine. For collection and replacement by Ambu..Furthermore, please instruct all customers of the received LOT(s), to check their devices for the wrong labelling as well Contact 800 262 8462 x 1121 or email [email protected] to arrange Return Authorization and replacement.

Distribution

US Nationwide, and country of Canada.

Quantity

267 units