IntelliVue MX700 patient monitor recall
IntelliVue MX700 patient monitor, model no. 865241
Why was IntelliVue MX700 patient monitor recalled?
Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.
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?
Serial numbers DE58562415 DE58562344 DE58562353
- Product
- IntelliVue MX700 patient monitor, model no. 865241
- Recalling firm
- Philips North America, LLC
- Quantity
- 28
- Distribution
- Domestic distribution to CA, HI, MA, NY, and UT. International distribution to Costa Rica, Ireland, Lebanon, and Poland.
- Recall date
- July 29, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)