FDA Device recall Z-2055-2025
Philips L12-4 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips L12-4 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-2055-2025 |
| 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 L12-4 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605427122, 989605451171, 989605434813, 989605434812, 989605477121, 989605434811; UDI: (01)00884838072305(2…Model No. 989605427122, 989605451171, 989605434813, 989605434812, 989605477121, 989605434811; UDI: (01)00884838072305(21)B1QJ17, (01)00884838061644(21)B2BBRN, (01)00884838061644(21)B1GL69, (01)00884838072305(21)B1YHN7, (01)00884838061644(21)B186QV, (01)00884838072305(21)B1QJ0G, (01)00884838072305(21)B21GPF, (01)00884838072305(21)B1QJ27, (01)00884838072305(21)B1QJ0V, (01)00884838061644(21)B14YT4, 010088483808516921B1L72F, (01)00884838072305(21)B21GNP, (01)00884838072305(21)B21GNR, (01)00884838072305(21)B1YHPV, (01)00884838072305(21)B21GRD, (01)00884838072305(21)B21GMK, (01)00884838085169(21)B1KFNJ, (01)00884838085169(21)B1QGTW, (01)00884838085169(21)B1L78H, (01)00884838072305(21)B1YHNZ, (01)00884838072305(21)B21GQ1, (01)00884838072305(21)B36LQZ, 010088483807230521B21GP4, (01)00884838072305(21)B1YHNK, 010088483808516921B27DYL, (01)00884838085169(21)B1XFGG, (01)00884838072305(21)B21GQH, (01)00884838072305(21)B329WD, (01)00884838085169(21)B1QGXP, (01)00884838072305(21)B21GQ6, (01)008848380 |
|---|
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-2055-2025%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.