Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by Philips Medical Systems, Inc. Due to VCG battery ignited in a VCG unit when...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems, Inc. directly.
Affected Products
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067. These rechargeable batteries are used to supply power to the following products: Wireless ECG Module used with the Precess MRI compatible Patient Monitoring System, Wireless SpO2 Module used with the Precess MRI Compatible Patient Monitoring System, Philips Basic Triggering Set, Philips Monitoring Sensor Set, Philips Battery Set
Quantity: 79
Why Was This Recalled?
VCG battery ignited in a VCG unit when recharging.
Where Was This Sold?
This product was distributed to 20 states: AL, CA, FL, GA, IL, MA, MN, NE, NJ, NY, NC, ND, OH, OR, PA, TN, TX, UT, WA, WI
About Philips Medical Systems, Inc.
Philips Medical Systems, Inc. has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report