Philips North America, LLC Phillips Module Charger, Product #: 989803191031 - Product Usage: This Module Charger is used in the Expression MR400 MRI Patient Monitoring System (Model MR400) is intended to monitor vital signs for patients undergoing MRI procedures and to provide signals for synchronization for the MRI scanner. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Phillips Module Charger, Product #: 989803191031 - Product Usage: This Module Charger is used in the Expression MR400 MRI Patient Monitoring System (Model MR400) is intended to monitor vital signs for patients undergoing MRI procedures and to provide signals for synchronization for the MRI scanner.
Brand
Philips North America, LLC
Lot Codes / Batch Numbers
Product #: 989803191031 Manufacturing date codes: prior to 2020-03
Products Sold
Product #: 989803191031 Manufacturing date codes: prior to 2020-03
Philips North America, LLC is recalling Phillips Module Charger, Product #: 989803191031 - Product Usage: This Module Charger is used in the due to A problem has been detected with the Philips LI-Polymer rechargeable battery when used with its approved charging station and module charger. When the. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A problem has been detected with the Philips LI-Polymer rechargeable battery when used with its approved charging station and module charger. When the battery is inserted into a charger bay, the LED indicatory lights solid red and the battery will not charge. This may result from poor electrical contact between the battery and charger.
Recommended Action
Per FDA guidance
Philips Healthcare sent a customer notification letter dated June 2020 explaining the potential issues observed with their products. This letter instructs the consumer to contact the company with any reports of issues associated with this failure.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026