NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Reported: June 7, 2017 Initiated: May 4, 2017 #Z-2175-2017
Product Description
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Reason for Recall
Manufacturing defect may cause localized heating, which may result in localized skin burn.
Details
- Recalling Firm
- Philips Electronics North America Corporation
- Units Affected
- 9120 devices
- Distribution
- US: AK AZ CA CO FL HI IA IL IN KY MA MD MI MN MO MS NC NE NH NJ NM NV NY OH OR PA TX VA WA WI WV OUS: Algeria Argentina Australia Austria Bahrain Belarus Belgium Bolivia Brazil Canada Chile China Colombia Costa Rica Denmark Dominican Rep Egypt Finland France Germany Hong Kong Hungary Iceland India Indonesia Ireland Israel Italy Japan Latvia Lebanon Libya Lithuania Luxembourg Malaysia Mexico Mongolia Netherlands New Zealand Norway Oman Pakistan Peru Philippines Poland Portugal Qatar Romania Russia Russian Fed. Saudi Arabia Singapore Slovenia South Africa South Korea Spain Sweden Switzerland Taiwan Thailand Tunisia Turkey Ukraine United Kingdom Utd.Arab.Emir.
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383). Recalled by Philips Electronics North America Corporation. Units affected: 9120 devices.
Why was this product recalled? ▼
Manufacturing defect may cause localized heating, which may result in localized skin burn.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 7, 2017. Severity: Moderate. Recall number: Z-2175-2017.
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