Philips Ingenuity TF UPS Accessory Devices Recalled for Battery Acid Leakage
Philips Medical Systems is recalling 14 Ingenuity TF UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (battery acid leakage, overheating, fumes) where injury has not yet been reported, which aligns with the High severity criteria.
Plain-English summary
Philips Medical Systems (Cleveland) Inc is recalling 14 units of Ingenuity TF Uninterruptible Power Supply (UPS) accessory devices. These devices are used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems.
The recall was initiated because the failure of these UPS accessory devices may result in battery acid leakage, overheating, and/or the emission of fumes. The affected units are identified by Model 882456 and specific serial numbers ranging from 2003 to 2018.
The affected devices were distributed worldwide, including the United States (nationwide, DC, and Puerto Rico) and numerous international locations. Consumers and healthcare facilities should contact the recalling firm for instructions on how to address the defect.
The recalled product
- Product
- Ingenuity TF (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
- Manufacturer
- Philips Medical Systems (Cleveland) Inc
- Category
- Medical Device — Imaging Systems
- Affected units
- 14
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (15)
- Model: 882456
- Serial #s: 2003
- 2004
- 2005
- 2006
- 2007
- 2008
- 2010
- 2011
- 2012
- 2013
- 2015
- 2016
- 2017
- 2018.
Distribution
Part of a larger recall action
This product is one of 35 recalled by Philips Medical Systems (Cleveland) Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 35 products in this recall →Related recalls
Same manufacturer · Philips Medical Systems (Cleveland) Inc
See all →- HighRadiation planning software recalled over image errors in three patient orientations
FDA (Devices) · 2025-09-24
- HighPinnacle 3 radiation planning software may miscalculate stopping power ratio
FDA (Devices) · 2025-08-13
- HighPinnacle3 Radiation Therapy Planning System dose-calculation software error
FDA (Devices) · 2022-09-21
- SeverePhilips Forte Gamma Camera System Recalled for Detector Fall Hazard
FDA (Devices) · 2019-11-13
- SeverePhilips Forte Gamma Camera System Recalled Due to Detector Falling Hazard
FDA (Devices) · 2019-11-13
Same hazard · chemical exposure
See all →- HighFDA Recalls Opportunity Pro Nitrile Gloves Due to Manufacturing Defects
FDA (Devices) · 2026-10-07
- HighFDA Recalls Performance Pro Nitrile Gloves Due to Defects
FDA (Devices) · 2026-10-07
- HighFDA Recalls Defective Blue Nitrile Patient Examination Gloves
FDA (Devices) · 2026-10-07
- ModerateSiemens Tricyclic Antidepressant Calibrator/Controls Recall Lot U2
FDA (Devices) · 2026-08-12
- LowSyva Emit Disopyramide Enzyme Immunoassay Calibrator Recalled for Sodium Azide Concentration
FDA (Devices) · 2026-08-12
Similar recalls
- HighPhilips Ingenuity TF PET/CT Systems Recalled for X-Ray Tube Oil Leakage
FDA (Devices) · 2018-07-04
- HighPhilips Ingenuity Core X-Ray Tube Recall for Oil Leakage Risk
FDA (Devices) · 2018-07-04
- HighPhilips Ingenuity TF PET/CT Software Recall for Potential Radiopharmaceutical Re-injection Risk
FDA (Devices) · 2013-11-06
- HighPhilips Ingenuity Core128 MRI Systems Recalled for X-Ray Tube Oil Leakage
FDA (Devices) · 2018-07-04
- HighPhilips Ingenuity Core128/Elite X-Ray Tube Recall for Oil Leakage
FDA (Devices) · 2018-07-04
- HighPhilips Ingenuity CT Software Recall for Performance Issues
FDA (Devices) · 2016-08-17