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.
Check against the official notice below — it lists the full affected range.
Philips North America, LLC has recalled 9,705 Module Chargers (Product #989803191031) used with the Expression MR400 MRI Patient Monitoring System. The chargers contain Philips LI-Polymer rechargeable batteries that experience a defect when inserted into a charger bay: the LED indicator light turns solid red and the battery will not charge. This problem results from poor electrical contact between the battery and charger. The affected units were manufactured prior to March 2020 and were distributed worldwide.
The recall documentation does not specify a remedy for consumers who have been affected by this product.
Written by software from the official notice below. Not reviewed by a lawyer.
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.
Reason for recall: 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. Distribution: World wide distribution. Firm reports distributing more product then quantity manufactured. Clarification requested. And received. Firm made error in counting number of batteries distributed. Quantity: 9,705 units Lot/code info: Product #: 989803191031 Manufacturing date codes: prior to 2020-03
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.