Philips Ingenuity CT Uninterruptible Power Supply Recall for Battery Acid Leakage
Philips is recalling 156 Ingenuity CT Uninterruptible Power Supply (UPS) accessory devices due to a risk 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 (battery acid leakage, overheating, fumes) from a medical device where no specific injuries or illnesses have been reported in the source text, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Philips Medical Systems (Cleveland) Inc is recalling 156 units of Ingenuity CT Uninterruptible Power Supply (UPS) accessory devices. These devices are used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. The recall covers units distributed in the United States (nationwide, including DC and Puerto Rico) and numerous countries worldwide.
The recall was initiated because the firm was notified that 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 # 728326 and specific serial numbers listed in the recall documentation.
Healthcare facilities and users of these devices should contact Philips Medical Systems (Cleveland) Inc for instructions on how to address the defect. The source text does not specify a particular consumer action beyond the general recall notification.
The recalled product
- Product
- Ingenuity CT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
- Manufacturer
- Philips Medical Systems (Cleveland) Inc
- Affected units
- 156
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 (20)
- Model #: 728326
- Serial #s: 30003
- 30005
- 30006
- 30007
- 30008
- 30009
- 30011
- 30012
- 30013
- 30014
- 30015
- 30018
- 30019
- 30022
- 30028
- 300003
- 300005
- 300010
- 300011
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.
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