Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
FDA Recall Z-0109-2019 · Posted None
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Recalling FirmBesmed Health Business Corporation
Recall StatusTerminated
Product CodeCAE
Date Initiated2018-08-09
Date Terminated2019-05-10
Product Quantity267 units
Reason for Recall
Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask Sterile
Firm 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.
Root Cause
Error in labeling
Distribution Pattern
US Nationwide, and country of Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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