Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray North America Due to Potential for a leak to occur on the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mindray DS USA, Inc. dba Mindray North America directly.
Affected Products
A7 Anesthesia Delivery System, a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic and to maintain a patient's ventilation. Part numbers 0632F-PA0000X (US domestic) and 0632B-00014 (international)
Quantity: 167 units (165 units - US) and (2 units - International)
Why Was This Recalled?
Potential for a leak to occur on the back-up O2 and air e-size cylinder yokes on the A7 Anesthesia Delivery System.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mindray DS USA, Inc. dba Mindray North America
Mindray DS USA, Inc. dba Mindray North America has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report