Philips Recalls BrightView SPECT UPS Accessory Devices for Safety Hazards
Philips Medical Systems is recalling 277 BrightView SPECT 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, fitting the 'High' severity criteria for theoretical hazards without confirmed illness or injury.
Plain-English summary
Philips Medical Systems (Cleveland) Inc is recalling 277 units of BrightView SPECT 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 worldwide, including the United States, DC, Puerto Rico, and numerous international locations.
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 emission of fumes. The specific model number is 882480, and the affected serial numbers are listed in the official recall documentation.
Healthcare facilities and users of these diagnostic imaging systems should check their equipment against the provided serial number list. If a device is affected, it should be removed from service and the manufacturer contacted for further instructions on repair or replacement.
The recalled product
- Product
- BrightView SPECT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
- Manufacturer
- Philips Medical Systems (Cleveland) Inc
- Affected units
- 277
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 #: 882480
- Serial #s: 466
- 4000031
- 4000048
- 4000077
- 4000132
- 4000186
- 4000251
- 4000296
- 4000323
- 4000336
- 4000381
- 4000390
- 4000403
- 4000404
- 4000405
- 4000406
- 4000407
- 4000414
- 4000415
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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