CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6030802, 7092001, 9042902, 9053001, 9061602, 9070702, 9081002, 9083101, 9083102, 9090301, 9090302, 9091101, 9092201, 9092202, 9101302, 9101901, 9102302, 9102801, 9102802, 9111601, 9111602, 9120902, 10020201, 10062906, 10071301, 10090201, 10090202, 10100501, 10100502, 10100701, 10100702, 10110303, 10110801, 10110802, 10120901, 10120902, 10121001, 10121002, 11021601, 11021602, 11031001, 11031002, 11041201, 11041202, 11051101, 11051102, 11070401, 11070402, 11072102, 11090801, 11090802, 11112301, 11120501, 11120502, 11121201, 11121202, 11121402, 12010601, 12012702, 12020101, 12020102, 12041201, 12052201, 12053001, 12053002, 12071101, 12071102, 12071201, 12071401, 110110804 & 110110806.
  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:

CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

Product Codes/Lot Numbers:

Model #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6030802, 7092001, 9042902, 9053001, 9061602, 9070702, 9081002, 9083101, 9083102, 9090301, 9090302, 9091101, 9092201, 9092202, 9101302, 9101901, 9102302, 9102801, 9102802, 9111601, 9111602, 9120902, 10020201, 10062906, 10071301, 10090201, 10090202, 10100501, 10100502, 10100701, 10100702, 10110303, 10110801, 10110802, 10120901, 10120902, 10121001, 10121002, 11021601, 11021602, 11031001, 11031002, 11041201, 11041202, 11051101, 11051102, 11070401, 11070402, 11072102, 11090801, 11090802, 11112301, 11120501, 11120502, 11121201, 11121202, 11121402, 12010601, 12012702, 12020101, 12020102, 12041201, 12052201, 12053001, 12053002, 12071101, 12071102, 12071201, 12071401, 110110804 & 110110806.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1784-2015

Related Recalls

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.

Aug 5, 2025 Other Medical Devices Nationwide View Details →