Drug recall
M3150 Information Center Local Database; Models: 862249, 865001, 865003, 865004, 865007, 865009, 865011…
FDA recall event 77437 · Class II · Philips Electronics North America Corporation
Key facts
| Event ID | 77437 |
|---|---|
| Recall numbers | Z-2528-2017 |
| Recalling firm | Philips Electronics North America Corporation |
| Product type | Devices |
| Products | M3150 Information Center Local Database; Models: 862249, 865001, 865003, 865004, 865007, 865009, 865011, 865012, 865091, 865092, 865093, 865094, 865095, 865096, 865098, 865099, 865102, 865104, 865105… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for early component failure. |
| Initiation date | Dec 17, 2010 |
| Report date | Jun 21, 2017 |
| Termination date | Aug 1, 2017 |
| 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: