FDA Device recall Z-2377-2025
L15-7io Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L15-7io Transducer Probe by Philips Ultrasound, citing to provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2377-2025 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2025-07-03 |
| Published | 2025-09-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
L15-7io Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605387852, 989605438421, 989605387341, 989605428532, 989605391083, 989605412042, 989605412082, 98960541896…Model No. 989605387852, 989605438421, 989605387341, 989605428532, 989605391083, 989605412042, 989605412082, 989605418963, 989605387851; UDI: (01)00884838061491(21)B2Y4MR, (01)00884838061491(21)B2YR9K, (01)00884838061491(21)F0DWM3, (01)00884838061491(21)F084NQ, (01)00884838061491(21)F0D244, (01)00884838061491(21)F0F19W, (01)00884838061491(21)F0G2RJ, (01)00884838061491(21)F0K6X7, (01)00884838087057(21)B2C14V, (01)00884838061491(21)B1PJC0, (01)00884838061491(21)B24YWK, (01)00884838061491(21)F0L51D, (01)00884838061491(21)F0L51F, (01)00884838061491(21)B31Q0J, (01)00884838061491(21)B3KQTR, (01)00884838061491(21)B2KLR3, (01)00884838061491(21)B2KLZ4, (01)00884838061491(21)B3H0PX, (01)00884838061491(21)B3J6LC, (01)00884838061491(21)F03BYJ, (01)00884838061491(21)F046Q9, (01)00884838061491(21)F04L49, (01)00884838061491(21)F0CXV3, (01)00884838061491(21)F0D5LN, (01)00884838061491(21)B1WGZP, (01)00884838061491(21)F03WVP, (01)00884838061491(21)F044Z4, (01)00884838073623(21)F041TJ, 010088483806149121F |
|---|
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-2377-2025%22
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