Philips recalls D2TCD Transducer Probes with specific model numbers for labeling clarification on useful life in medical ultrasound field use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain D2TCD Transducer Probes to clarify their useful life labeling for medical ultrasound field use. This recall addresses labeling to ensure proper understanding of how long these probes remain functional in clinical settings.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. This ensures medical professionals understand the expected lifespan of the probes for safe and effective clinical use without causing harm.
Medical professionals using Philips D2TCD Transducer Probes with the listed model numbers are affected. Patients using these probes for ultrasound imaging may be at low risk if the labeling clarification is properly implemented.
Check for model numbers 989605412102 or 989605438591 on the probe. Also, look for the unique identifiers (UDI) listed in the recall notice to confirm if your probe is affected.
Verify your D2TCD Transducer Probe has model numbers 989605412102 or 989605438591.
Ensure the probe's labeling clearly states the useful life for medical ultrasound field use as per Philips' clarification.
Philips is recalling these transducers to clarify the useful life labeling for medical ultrasound field use, ensuring proper understanding of their expected lifespan.
No, the recall does not require stopping use. The labeling clarification is for better understanding of useful life without immediate action needed.
Check for model numbers 989605412102 or 989605438591, or the unique identifiers (UDI) listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2367-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2367-2025 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.
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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.
