IntelliVue MX800 patient monitor, model no. 865240
Reported: July 29, 2020 Initiated: June 30, 2020 #Z-2696-2020
Product Description
IntelliVue MX800 patient monitor, model no. 865240
Reason for Recall
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.
Details
- Recalling Firm
- Philips North America, LLC
- Units Affected
- 28
- Distribution
- Domestic distribution to CA, HI, MA, NY, and UT. International distribution to Costa Rica, Ireland, Lebanon, and Poland.
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
IntelliVue MX800 patient monitor, model no. 865240. Recalled by Philips North America, LLC. Units affected: 28.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 29, 2020. Severity: Moderate. Recall number: Z-2696-2020.
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