Philips Expression MR200 MRI Patient Monitoring System — Class II medical device recall Z-0069-2015
Terminated recall by Invivo Corporation, reported 2014-10-22, distributed in CA, GA, MI, NJ, NV, TX. Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.
| Recall number | Z-0069-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invivo Corporation, Orlando, FL, United States |
| Recall initiated | 2014-09-05 |
| Classified | 2014-10-15 |
| Reported by FDA | 2014-10-22 |
| Terminated | 2017-10-12 |
| Distributed | CA, GA, MI, NJ, NV, TX |
| Countries outside the US | AT, CH, DE, FI, GB, PL, SE, SG |
| Quantity | 24 units |
| 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 |
| Model numbers | 866120 |
Product
Philips Expression MR200 MRI Patient Monitoring System
Reason for recall
Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0069-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.