🔍 RecallPedia

Ingenuity Core 128 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

Class I - Dangerous
🏥 Medical Devices Recalled: March 6, 2015 Philips Medical Systems (Cleveland) Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    Model #: 728323; Serial #s: 30153, 32002, 32003, 32004, 32005, 32006, 32007, 32009, 32010, 32011, 32013, 32014, 32015, 32016, 32018, 32021, 32023, 32025, 32026, 32029, 32030, 32031, 32032, 32033, 32034, 32035, 32036, 32037, 32038, 32040, 32041, 32042, 32043, 32044, 32046, 32047, 32048, 32049, 32051, 32052, 32053, 32054, 32057, 32059, 32060, 32062, 32064, 32066, 32068, 32069, 32070, 32072, 32073, 32074, 32077, 32078, 32080, 32083, 32084, 32089, 32091, 32092, 32094, 32095, 32098, 32100, 32101, 32104, 32106, 32107, 32108, 300137, 310067, 320001, 320002, 320003, 320004, 320005, 320006, 320007, 320008, 320009, 320010, 320011, 320013, 320014, 320015, 320018, 320019, 320020, 320021, 320022, 320023, 320024, 320025, 320026, 320027, 320028, 320029, 320030, 320031, 320032, 320033, 320034, 320035, 320036, 320037, 320038, 320039, 320040, 320041, 320043, 320044, 320045, 320046, 320047, 320048, 320049, 320050, 320051, 320052, 320053, 320054, 320055, 320056, 320057, 320059, 320060, 320062, 320063, 320064, 320065, 320066, 320067, 320068, 320069, 320070, 320071, 320072, 320073, 320074, 320075, 320076, 320077, 320078, 320079, 320080, 320081, 320082, 320083, 320084, 320085, 320086, 320087, 320088, 320089, 320090, 320092, 320093, 320095, 320096, 320097, 320098, 320099, 320101, 320102, 320103, 320104, 320105, 320106, 320107, 320109, 320110, 320111, 320112, 320114, 320115, 320116, 320117, 320118, 320119, 320120, 320121, 320122, 320123, 320124, 320125, 320126, 320128, 320129, 320131, 320132, 320133, 320134, 320135, 320137, 320138, 320139, 320140, 320141, 320142, 320143, 320144, 320145, 320146, 320147, 320148, 320150, 336001, 336002, 336003, 336006, 336007, 336008, 336009, 336010, 336011, 336012, 336013, 336014, 336015, 336016, 336018, 336020, 336021, 336024, 336027, 336028, 336029, 336030, 336031, 336032, 336033, 336034, 336035, 336036, 336037, 336038, 336039, 336040, 336042, 336043, 336044, 336046, 336047, 336048, 336050, 336052, 336055, 336056, 336057, 336058, 336059, 336061, 336063, 336066, 336067, 336068, 336069, 336070, 336071, 336072, 336074, 336075, 336076, 336080, 336081, 336086, 336087, 336089, 336702, 336703, 336704, 336705, 336706, 336708, 336709, 336710, 336711, 336713, 336714, 336715, 336716, 336717, 336718, 336719, 336721, 336707
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Philips Medical Systems (Cleveland) Inc
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Ingenuity Core 128 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

Product Codes/Lot Numbers:

Model #: 728323; Serial #s: 30153, 32002, 32003, 32004, 32005, 32006, 32007, 32009, 32010, 32011, 32013, 32014, 32015, 32016, 32018, 32021, 32023, 32025, 32026, 32029, 32030, 32031, 32032, 32033, 32034, 32035, 32036, 32037, 32038, 32040, 32041, 32042, 32043, 32044, 32046, 32047, 32048, 32049, 32051, 32052, 32053, 32054, 32057, 32059, 32060, 32062, 32064, 32066, 32068, 32069, 32070, 32072, 32073, 32074, 32077, 32078, 32080, 32083, 32084, 32089, 32091, 32092, 32094, 32095, 32098, 32100, 32101, 32104, 32106, 32107, 32108, 300137, 310067, 320001, 320002, 320003, 320004, 320005, 320006, 320007, 320008, 320009, 320010, 320011, 320013, 320014, 320015, 320018, 320019, 320020, 320021, 320022, 320023, 320024, 320025, 320026, 320027, 320028, 320029, 320030, 320031, 320032, 320033, 320034, 320035, 320036, 320037, 320038, 320039, 320040, 320041, 320043, 320044, 320045, 320046, 320047, 320048, 320049, 320050, 320051, 320052, 320053, 320054, 320055, 320056, 320057, 320059, 320060, 320062, 320063, 320064, 320065, 320066, 320067, 320068, 320069, 320070, 320071, 320072, 320073, 320074, 320075, 320076, 320077, 320078, 320079, 320080, 320081, 320082, 320083, 320084, 320085, 320086, 320087, 320088, 320089, 320090, 320092, 320093, 320095, 320096, 320097, 320098, 320099, 320101, 320102, 320103, 320104, 320105, 320106, 320107, 320109, 320110, 320111, 320112, 320114, 320115, 320116, 320117, 320118, 320119, 320120, 320121, 320122, 320123, 320124, 320125, 320126, 320128, 320129, 320131, 320132, 320133, 320134, 320135, 320137, 320138, 320139, 320140, 320141, 320142, 320143, 320144, 320145, 320146, 320147, 320148, 320150, 336001, 336002, 336003, 336006, 336007, 336008, 336009, 336010, 336011, 336012, 336013, 336014, 336015, 336016, 336018, 336020, 336021, 336024, 336027, 336028, 336029, 336030, 336031, 336032, 336033, 336034, 336035, 336036, 336037, 336038, 336039, 336040, 336042, 336043, 336044, 336046, 336047, 336048, 336050, 336052, 336055, 336056, 336057, 336058, 336059, 336061, 336063, 336066, 336067, 336068, 336069, 336070, 336071, 336072, 336074, 336075, 336076, 336080, 336081, 336086, 336087, 336089, 336702, 336703, 336704, 336705, 336706, 336708, 336709, 336710, 336711, 336713, 336714, 336715, 336716, 336717, 336718, 336719, 336721, 336707

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1772-2015

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Philips Medical Systems (Cleveland)

Class I - Dangerous

Due to a software issue, there is a potential image error of the Region of Interest for expansion/contraction for HFP (Head First Prone), FFS (Feet First Supine) and FFP (Feet First Prone) orientations.

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