Besmed Health recalls Ambu Aura40 Standard reusable laryngeal masks due to potential infection risk from improper sterilization. Affected units have specific catalog and lot numbers.
Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked AuraStraight Silicone, Single Use Laryngeal Mask Sterile
Besmed Health is recalling Ambu Aura40 Standard reusable laryngeal masks because they may not be properly sterilized, increasing infection risk. This affects medical professionals using the masks for airway management.
The masks are designed to be reused but require specific sterilization procedures. If not properly sterilized, they can become contaminated and cause infections. This risk is particularly concerning in medical settings where masks are used repeatedly.
Medical professionals who use the Ambu Aura40 Standard laryngeal masks for airway management during procedures. Patients receiving care with these masks are at risk if the masks are not properly sterilized.
Check for the catalog number 340300000 and lot numbers MO0612G40021 or MO0605G40014 on the packaging. The masks are labeled as 'AuraStraight Silicone, Single Use Laryngeal Mask Sterile' in a pouch.
Look for catalog number 340300000 and lot numbers MO0612G40021 or MO0605G40014 on the packaging.
The Ambu Aura40 Standard reusable laryngeal masks may not be properly sterilized, increasing the risk of infection.
Check the product details for the catalog number and lot numbers. If you have the affected units, contact Besmed Health for guidance.
If not properly sterilized, the masks can become contaminated and cause infections, especially in medical settings.
We’ve drafted a message you can send Besmed Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0109-2019 — Besmed Health Besmed Health Hello, I own a Besmed Health that is covered by recall Z-0109-2019 from Besmed Health. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
