FDA Device recall Z-2054-2025
Philips L12-3 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips L12-3 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-2054-2025 |
| 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 L12-3 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No.989605412072, 989605412071, 989605438571, 989605348241; UDI: (01)00884838061620(21)B0TLJT, (01)00884838061620…Model No.989605412072, 989605412071, 989605438571, 989605348241; UDI: (01)00884838061620(21)B0TLJT, (01)00884838061620(21)B10GRD, (01)00884838061620(21)B0PYG5, (01)00884838061620(21)B0HF63, (01)00884838061620(21)B0WMR0, (01)00884838061620(21)B15HGH, (01)00884838061620(21)B0Q3CK, (01)00884838061620(21)B0K211, (01)00884838061620(21)B138Y9, (01)00884838061620(21)B11C62, (01)00884838061620(21)B0NK8H, (01)00884838061620(21)B1396N, (01)00884838061620(21)B139FV, (01)00884838061620(21)B0PY5N, (01)00884838061620(21)B16XQR, (01)00884838061620(21)B126FZ, (01)00884838061620(21)B18R5Q, (01)00884838061620(21)B0QKNF, (01)00884838061620(21)B0R3XG, (01)00884838061620(21)B0QN7N, (01)00884838061620(21)B14ZY4, (01)00884838061620(21)B18R9K, (01)00884838061620(21)B1500H, (01)00884838061620(21)B1KB6Q, (01)00884838061620(21)B15NHL, (01)00884838061620(21)B170P0, (01)00884838061620(21)B1CPKD, (01)00884838061620(21)B0TKYJ, (01)00884838061620(21)B144FW, (01)00884838061620(21)B10QGD, (01)00884838061620(21)B13W02, |
|---|
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-2054-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.