Drug recall
Philips 3D9-3v Transducer.
FDA recall event 96994 · Class II · Philips Ultrasound, Inc
Key facts
| Event ID | 96994 |
|---|---|
| Recall numbers | Z-2048-2025, Z-2049-2025, Z-2050-2025, Z-2051-2025, Z-2052-2025, Z-2053-2025, Z-2054-2025, Z-2055-2025, Z-2056-2025, Z-2057-2025, Z-2058-2025, Z-2059-2025 and 9 more |
| Recalling firm | Philips Ultrasound, Inc |
| Product type | Devices |
| Products | Philips 3D9-3v Transducer., Philips C5-1 Transducer., Philips C5-2 Transducer., Philips C9-5EC Transducer., Philips eL18-4 EMT Transducer. and 16 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Ultrasound transducer devices were refurbished beyond their useful life. |
| Initiation date | May 28, 2025 |
| Report date | Jul 9, 2025 |
| City | Reedsville |
| State | PA |
| Country | United States |
| FEI number | 2518586 |
At a glance
- 10–99 Products in this recall
- 1–9 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: