Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module Recalled by Philips Electronics North America Corporation Due to Manufacturing defect may cause localized heating, which may...
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 Electronics North America Corporation directly.
Affected Products
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Quantity: 9120 devices
Why Was This Recalled?
Manufacturing defect may cause localized heating, which may result in localized skin burn.
Where Was This Sold?
This product was distributed to 31 states: AK, AZ, CA, CO, FL, HI, IL, IN, IA, KY, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NM, NY, NC, OH, OR, PA, TX, VA, WA, WV, WI
About Philips Electronics North America Corporation
Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report