FDA Device recall Z-2052-2025
Philips eL18-4 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips eL18-4 Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2052-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-28 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
Philips eL18-4 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No.989605456291, 989605431531; UDI: (01)00884838070813(21)B2JXFM, (01)00884838070813(21)B25L9M, (01)0088483807081…Model No.989605456291, 989605431531; UDI: (01)00884838070813(21)B2JXFM, (01)00884838070813(21)B25L9M, (01)00884838070813(21)B25LJ0, (01)00884838070813(21)B25LY7, (01)00884838070806(21)B29W04; Serial No. B2JXFM, B25L9M, B28MJZ, B25LJ0, B25LY7, B29W04. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2052-2025%22
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