Invivo Corporation recalls
Every recall we track for Invivo Corporation — 9 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Invivo Corporation peaked in 2018 (4); 9 since 2017.
All FDA recall records for Invivo Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 2 | 1 | 0 | 3 |
| 2018 | 0 | 0 | 4 | 0 | 4 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Invivo Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Invivo Corporation recalls
9 shown- Lower riskMedical device
Invivo Corporation recalls MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic
Invivo Corporation recalls MR Coils with mistakenly printed IPX1 water rating labels. These coils are used with MRI scanners. Affected models include dS Knee Sch 1.5T, dS Shoulder Sch 3.0T, and others. No action is required as the labels are incorrect but not dangerous.
InvivoSep 14, 2020 - Lower riskMedical device
Invivo Corporation recalls Monitor for the Functional Imaging System for Magnetic Resonance Imaging System
Invivo recalls specific MRI monitor models due to insufficient shielding of Philips SensaVue DVI Adapter, which may cause interference with MRI safety systems.
InvivoFeb 6, 2020 - Lower riskMedical device
Invivo Corporation recalls Xper Flex Cardio Physiomonitoring System, Software version 1.6.0.0388
Invivo recalls Xper Flex Cardio Physiomonitoring System software version 1.6.0.0388 due to potential freezing of invasive blood pressure readings during certain actions. Affected units have specific serial numbers listed in the recall notice.
InvivoSep 24, 2018 - Lower riskMedical device
Invivo Corporation recalls Xper Flex Cardio Physiomonitoring System Model # 453564669081 Software Version 1.6.0.0388
Invivo recalls Xper Flex Cardio Physiomonitoring System with faulty software version 1.6.0.0388 that may cause inaccurate ECG readings and heart rate displays. Affected units have specific serial numbers listed in the recall.
InvivoAug 3, 2018 - Lower riskMedical device
Invivo Corporation recalls PHILIPS Xper Flex Cardio Physiomonitoring System, Model Numbers: 453564241901, 453564483321, 453564621791, and
US1433000052
US1433000052Mar 14, 2018 - Lower riskMedical device
Invivo Corporation recalls DynaCad software consist of an MR Analysis Server software and the viewer workstation software. The MR Analysis
Invivo recalls DynaCad software updates 3.5 causing incorrect pharmacokinetic and diffusion maps. Users may underestimate critical medical values. No remedy stated.
InvivoJan 24, 2018 - Lower riskMedical device
Invivo Corporation recalls Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive
Invivo recalls Xper Flex Cardio Physiomonitoring System units with specific serial numbers due to a potential issue where pressing ESC key accidentally closes Full Disclosure Control Window during playback.
InvivoNov 20, 2017 - Use cautionMedical device
Invivo Corporation recalls Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive investigations of heart and vascular disease when
Invivo recalls Xper Flex Cardio Physiomonitoring systems with intermittent communication between host and FlexCardio. Affected models include Revision A/B with specific serial numbers. Stop using immediately to prevent potential device malfunction.
InvivoAug 18, 2017 - Use cautionMedical device
Invivo Corporation recalls Xper Flex Cardio PhysioMonitoring system The Xper Flex Cardio physiomonitoring system is used to facilitate invasive
Invivo recalls Xper Flex Cardio devices with intermittent communication between host system and Flex Cardio. This may cause inaccurate readings during heart and vascular monitoring. Affected models include 453564621791 and :453564621801 (Revision C).
InvivoAug 11, 2017
Invivo Corporation recall questions
How many recalls has Invivo Corporation had?
9 recalls from Invivo Corporation are on record with U.S. safety agencies, from 2017–2020.
What is the most recent Invivo Corporation recall?
Invivo Corporation recalls MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic, dated Sep 14, 2020. Every Invivo Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Invivo Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Invivo Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.