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Philips Electronics North America Corporation recalls NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Recalled June 7, 2017 · FDA recall Z-2175-2017 · Philips Electronics North America
Hazard
Manufacturing defect may cause localized heating, which may result in localized skin burn. · FDA Class II
Units
9120 devices
Sold at
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Description
Manufacturing defect may cause localized heating, which may result in localized skin burn.
Product
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Manufacturer(s)
Philips Electronics North America Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →