FDA recall record

Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray DS USA Inc. 800 recall — FDA Z-0291-2013

Mindray has identified the potential for a system leak resulting an issue related to the carbon dioxide absorber canister gasket on A3/A5 Anesthesia…

Class Iclassification
Z-0291-2013official record ID
Nov 28, 2012report date

Recall record at a glance

Official recordZ-0291-2013
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMindray DS USA, Inc. d.b.a. Mindray North America
Report dateNov 28, 2012
Recall initiation dateAug 13, 2012
Quantity346 units (311 US - 35 Foreign)
LocationMahwah, NJ, United States

Official product description

Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray DS USA Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 This is a device used to administer to a patient continuously or intermittently a general inhalation anesthetic and to maintain a patient's ventilation.

Why the product was recalled

Mindray has identified the potential for a system leak resulting an issue related to the carbon dioxide absorber canister gasket on A3/A5 Anesthesia Delivery Systems. A potential system leak resulting from the canister gasket will likely present itself during the Automatic Circuit Leak and Compliance Test performed at startup and the Manual Leak Test recommended to be performed before each case.

Distribution information

Worldwide distribution: USA (nationwide) including Puerto Rico and countries of: Australia, Chile, Colombia, and Venezuela.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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