Monitor for the Functional Imaging System for Magnetic Resonance… — Class II medical device recall Z-1440-2020
Terminated recall by Invivo Corporation, reported 2020-03-11, distributed in AK, AL, CA, CO, FL, IL, IN, KY…. Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
| Recall number | Z-1440-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invivo Corporation, Gainesville, FL, United States |
| Recall initiated | 2020-02-06 |
| Classified | 2020-03-04 |
| Reported by FDA | 2020-03-11 |
| Terminated | 2022-05-04 |
| Distributed | AK, AL, CA, CO, FL, IL, IN, KY, MA, MI, NY, OH, OR, PA, TN, TX, WV |
| Countries outside the US | AU, CA, FR, GB, IN, IT, JP, NL, SA, TH |
| Quantity | 75 |
Product
Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
Reason for recall
Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
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-1440-2020. 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.