Mindray DS USA, Inc. dba Mindray North America Recalls

2 recalls found for Mindray DS USA, Inc. dba Mindray North America. Check if any of your products are affected.

HIGHFDA DEVICE

Mindray Recalls Anesthesia System Over Leakage Risk

Mindray DS USA, Inc. recalled 148 units of the V90 Electronic Vaporizer on October 20, 2025. The recall follows reports of potential anesthesia leakage that could impact patient safety. Healthcare providers and patients must stop using the device immediately.

Mindray DS USA, Inc. dba Mindray North America
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HIGHFDA DEVICE

Mindray Vaporizer Recalled Due to Anesthesia Leakage Risk

Mindray DS USA, Inc. recalled 54 units of the Isoflurane V90 Electronic Vaporizer on October 20, 2025. The recall stems from a potential anesthesia leakage issue that poses serious health risks. Affected devices were distributed in the U.S. and Canada.

Mindray DS USA, Inc. dba Mindray North America
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Brand Statistics

Total Recalls
2
Pages
1