Drug recall
Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;
FDA recall event 96889 · Class II · Philips North America Llc
Key facts
| Event ID | 96889 |
|---|---|
| Recall numbers | Z-1788-2025, Z-1789-2025, Z-1790-2025, Z-1791-2025, Z-1792-2025, Z-1793-2025, Z-1794-2025, Z-1795-2025, Z-1796-2025, Z-1797-2025, Z-1798-2025, Z-1799-2025 and 6 more |
| Recalling firm | Philips North America Llc |
| Product type | Devices |
| Products | Product Name: Evolution Upgrade 1.5T; Model Numbers: (1) 782116, (2) 782148;, Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;, Product Name: Ingenia 1.5T CX; Model Number: 781262;, Product Name: Ingenia 1.5T; Model Numbers: (1) 781315, (2) 781341, (3) 781396, (4) 782101, (5) 782115, (6) 782140;, Product Name: Ingenia 1.5T S; Model Number: 781347; and 13 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. |
| Initiation date | May 13, 2025 |
| Report date | May 28, 2025 |
| City | Cambridge |
| State | MA |
| Country | United States |
| FEI number | 3016618143 |
At a glance
- 10–99 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: