Forte-JetStream AZ (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Check against the official notice below — it lists the full affected range.
Philips Medical Systems is recalling Forte-JetStream AZ uninterruptible power supply (UPS) accessory devices used with Computed Tomography X-ray systems and Diagnostic Imaging systems due to a hazard involving failure of the UPS devices that may cause battery acid leakage, overheating, and/or emission of fumes. A total of 11 units with model number 882320 have been distributed worldwide, including throughout the United States, Puerto Rico, and numerous other countries.
The affected devices are identified by specific serial numbers: 1000508, 10000502, 10000504, 10000506, 10000507, 10007040410, B04070065, FA04120026, FA04120029, FA06010213, and FA06110355. The record does not specify a remedy or recommend any action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
The firm was notified that the failure of the UPS accessory devices used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. may result in battery acid leakage, overheating and/or emission of fumes.
Reason for recall: The firm was notified that the failure of the UPS accessory devices used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. may result in battery acid leakage, overheating and/or emission of fumes. Distribution: Worldwide Distribution-US (nationwide) including DC & Puerto Rico and the following countries: Albania, Algeria, Argentina, Australia, Austria, Bangladesh, Belgium, Bolivia, Brazil, Bulgaria, Cambodia, Cameroon, Cayman Islands, China, Colombia, Democratic Congo, Croatia, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Ethiopia, Finland, France, Gabon, Georgia, Germany, Ghana, Gr Quantity: 11 units Lot/code info: Model #: 882320; Serial #s: 1000508, 10000502, 10000504, 10000506, 10000507, 10007040410, B04070065, FA04120026, FA04120029, FA06010213 & FA06110355.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.