Mindray DS USA announces voluntary recall of A3/A5 Anesthesia Delivery System Mindray Medical International Ltd has initiated a voluntary recall affecting the A3/A5 Anesthesia Delivery System. Mindray has initiated this recall due to the possibility of a system leak resulting from improper seating of the CO2 absorbent canister gasket. To date, approximately 70% of units affected by this action have been corrected. The issue is corrected through a replacement of the canister gasket by a Mindray Service or authorized representative. Units with the affected canister gaskets were shipped between May 31, 2011 and July 15, 2012 in the U.S., Latin America and Australia. There have been no reports of injuries associated with this issue. Mindray became aware of the issue when a system leak was reported by a customer. The cause of the leak was determined to be the result of an improperly seated canister gasket. Mindray has advised the U.S. FDA of this voluntary recall.
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