Invivo Corporation Recalls

All product recalls associated with Invivo Corporation.

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Recall Summary

Total Recalls

7

Past Year

0

Class I (Serious)

0

Most Recent

Sep 2020

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–7 of 7 recalls

MR Coils (Invivo) – label rating error (2020)

The labels have been mistakenly printed with an IPX1 rating symbol. IPX ratings relate to protections that products have from water ingress.

Low

FDASep 14, 2020Nationwide• Invivo Corporation

MRI System Monitor (Invivo) – insufficient shielding (2020)

Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.

Low

FDAFeb 6, 2020AL, AK, CA +14 more• Invivo Corporation

Philips Expression MR200 (Invivo) – Power Test Failure (2014)

The MR 200 devices failed the initial power up test due to capacitor short and hi-pot testing; possible loss of Patient Monitoring or User/Service Electrical Shock.

Class IIModerate

FDA

Oct 22, 2014

CA, FL, IN +8 more

• Invivo Corporation

Expression Information Portal (Invivo) – Display Freezing (2014)

Frozen Display Numerics and Disabled Menu Keys after extended run time. This customer notification was sent August 22, 2014.

Class IIModerate

FDASep 14, 2014Nationwide• Invivo Corporation

Philips Expression MR200 (Invivo) – Metal Debris Risk (2014)

During production, excess metal (aluminum) debris was found stuck to the cling plastic that covers the device's pole assembly. The metallic debris could affect system performance due to the potential for a failure to power up or loss of power. This could result in the loss of monitoring and a delay in diagnosis of the patient.

Class IIModerate

FDASep 8, 2014CA, IN• Invivo Corporation

Philips Expression MR200 (Invivo) – Blood Pressure Failure (2014)

Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.

Class IIModerate

FDASep 5, 2014CA, GA, MI +3 more• Invivo Corporation

Invivo Corporation: 3.7 V Li-Polymer Battery, used in Precess MRI Compatible ...

Battery Failure: The Invivo Lithium Polymer Wireless Module Battery Part Number 9065 and the Lithium Polymer Fiber Optic Module Battery Part Number 9067 is being recalled because the battery, itself, when dropped from 3 feet/1 meter onto a hard surface can produce a flame and then emit smoke. The firms investigation shows that the battery failure does not occur when a module is dropped with a ba

FDAAug 13, 2008Nationwide• Invivo Corporation

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Invivo Corporation Recalls

Recall Summary

MR Coils (Invivo) – label rating error (2020)

MRI System Monitor (Invivo) – insufficient shielding (2020)

Philips Expression MR200 (Invivo) – Power Test Failure (2014)

Expression Information Portal (Invivo) – Display Freezing (2014)

Philips Expression MR200 (Invivo) – Metal Debris Risk (2014)

Philips Expression MR200 (Invivo) – Blood Pressure Failure (2014)

Invivo Corporation: 3.7 V Li-Polymer Battery, used in Precess MRI Compatible ...