FDA Device recall Z-0069-2015
Philips Expression MR200 MRI Patient Monitoring System
- FDA Device
- Class II
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class II recall of Philips Expression MR200 MRI Patient Monitoring System by Invivo, citing failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0069-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-09-05 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Invivo |
| Distribution | CA, GA, MI, NJ, NV, TX |
Product
Philips Expression MR200 MRI Patient Monitoring System
Reason
Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.
Identifiers
| code_info | Model: 866120, Lot numbers: US33600004, US33600005, US33600006, US33600007, US33600008, US33600009, US33600010, US336…Model: 866120, Lot numbers: US33600004, US33600005, US33600006, US33600007, US33600008, US33600009, US33600010, US33600011, US33600012, US33600013, US33600014, US33600015, US33600016, US33600017, US33600018, US33600019, US33600020, US33600022, US33600023, US33600024, US33600025, US33600026, US33600027, US33600028. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0069-2015%22
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