Philips recalls L12-4 Transducer Probes with specific model numbers for clarification on useful life labeling in the field. No safety hazard exists; this is a labeling update to help users understand product lifespan.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain L12-4 Transducer Probes to update labeling about their useful life in the field. This is not a safety hazard but a clarification for users to better understand how long these probes should be used before replacement.
This recall is for labeling clarification only. There is no safety hazard or risk of injury. Philips is updating the labeling to help users understand the useful life of these transducers in the field.
Users of Philips L12-4 Transducer Probes with the listed model numbers are affected. This recall does not pose a safety risk but helps clarify the product's intended lifespan.
Check your L12-4 Transducer Probe for model numbers: 989605430652, 989605409562, 989605427122, and other specific numbers listed in the recall. Also check the UDI codes provided in the recall notice.
Review your L12-4 Transducer Probe's model number to see if it matches the listed numbers in the recall.
Philips has updated labeling to clarify the useful life of these transducers in the field; no action is needed beyond understanding the new labeling.
No, this recall is for labeling clarification only. There is no safety hazard or risk of injury.
No action is needed. Philips is updating labeling to help users understand the useful life of these transducers in the field.
The affected model numbers are listed in the recall: 989605430652, 989605409562, 989605427122, and other specific numbers provided 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-2373-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2373-2025 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.
