Drug recall
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
FDA recall event 77166 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 77166 |
|---|---|
| Recall numbers | Z-2175-2017 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383) |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Manufacturing defect may cause localized heating, which may result in localized skin burn. |
| Initiation date | May 4, 2017 |
| Report date | Jun 7, 2017 |
| Termination date | Jun 28, 2018 |
| City | Andover |
| State | MA |
| Country | United States |
| FEI number | 1218950 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: