Mindray DPM5 Monitor recall
Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
Why was Mindray DPM5 Monitor recalled?
Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
p/n 9201F-PA000XX DS- 0C000565 02000335 12000603 12000599 12000597 OCOOO569 9A000247 9A000252 17000648 06000490 05000470 05000466 02000373
- Product
- Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities.
- Recalling firm
- Mindray DS USA, Inc. d.b.a. Mindray North America
- Quantity
- 13 units
- Distribution
- US Nationwide Distribution including the states of: VA, TN, FL, & TX
- Recall date
- February 6, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)