Philips recalls Mini Multi TEE Transducer Probe models with specific serial numbers due to labeling for field use duration. This recall provides clarity on transducer lifespan without safety risks.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain Mini Multi TEE Transducer Probes to clarify their useful life in medical settings. This recall helps healthcare providers understand how long these ultrasound probes should be used before replacement.
The recall focuses on labeling the useful life of ultrasound transducers in the field. This ensures healthcare providers know when to replace probes to maintain accurate imaging. There is no safety hazard described in the recall.
Healthcare professionals using Philips Mini Multi TEE Transducer Probes with the listed serial numbers or model codes are affected. Patients using these probes under medical supervision are not at risk.
Check for serial numbers like 0341YT, 0319CQ, or model codes 989605439242 and 21381A on the probe. The recall specifies these identifiers for affected units.
Verify your probe's serial number against the listed codes: 0341YT, 0319CQ, 028NZW, B0RF1J, B0F31L, B0DTV4, B0C9XR, 02H0L8, B0KYGV, B01639, B06NT3, 03C68B, 03C8CW.
Philips is recalling these probes to clarify their useful life in medical settings, ensuring healthcare providers know when to replace them for accurate imaging.
The recall does not mention any safety hazards. It focuses on labeling the useful life of the transducers to help with proper usage.
Check for serial numbers like 0341YT, 0319CQ, or model codes 989605439242 and 21381A on the probe.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2385-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2385-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
