Philips recalls L12-5 Transducer Probe model 989605408174 for labeling clarity on useful life in field use. No immediate safety risk.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling its L12-5 Transducer Probe model 989:605408174 due to labeling issues for field use duration. This does not pose a safety risk but ensures proper usage guidance.
The recall addresses labeling clarity for the transducer's useful life in field conditions. Without clear labeling, users might misinterpret how long the probe remains functional, potentially leading to improper usage decisions.
Users of Philips L12-5 Transducer Probes with model number 989605408174 are affected. Medical professionals using these probes for ultrasound imaging are most at risk of misinterpretation.
Check for model number 989605408174 on the transducer probe. This model was sold by Philips Ultrasound, Inc.
Verify the model number on the transducer probe to confirm if it matches 989605408174.
Philips is recalling this model for labeling clarity to define the useful life of ultrasound transducers in field use.
No, the recall is for labeling clarification only and does not pose a safety risk.
Check for model number 989605408174 on the transducer probe.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2402-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2402-2025 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.
