Z-2697-2020 Class II Terminated
FDA device recall Z-2697-2020 was initiated by Philips North America, LLC on June 30, 2020 and is designated Class II. 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… The recall status is terminated (terminated January 25, 2024). Affected quantity: 28.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2020
- Initiation Date
- June 30, 2020
- Termination Date
- January 25, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 28
Product Description
IntelliVue MX700 patient monitor, model no. 865241
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.
Distribution Pattern
Domestic distribution to CA, HI, MA, NY, and UT. International distribution to Costa Rica, Ireland, Lebanon, and Poland.
Code Information
Serial numbers DE58562415 DE58562344 DE58562353