Philips Electronics North America Corporation recalls NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
- Recall date
- May 4, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2175-2017
- FDA classification
- Class II
- Brand / firm
- Philips Electronics North America Corporation
- Sold / distributed
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Why it was recalled
Manufacturing defect may cause localized heating, which may result in localized skin burn.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
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