Philips recalls X6-1 Transducer Probes with specific model numbers for labeling clarification on useful life 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 X6-1 Transducer Probes with specific model numbers to clarify labeling about their useful life in the field. This is not a safety hazard but a labeling update to help users understand how long the product is expected to function.
The recall is for labeling clarification on the useful life of the transducers in the field. There is no safety hazard described; this is a labeling update to help users understand the expected lifespan of the product.
Users of Philips X6-1 Transducer Probes with the listed model numbers. The recall does not pose a safety risk but aims to improve labeling clarity for product lifespan.
Check your X6-1 Transducer Probe for model numbers 989605409282, 989605438511, 989605357141, 989605357143, 989605427801 or UDI codes starting with (01)00884838061446(21) followed by specific sequences.
Identify your X6-1 Transducer Probe model number or UDI code to confirm if it's in the recall list.
No, this recall is for labeling clarification on the useful life of the transducers in the field. There is no safety hazard.
No action is required. This is a labeling update to help users understand the product's expected lifespan.
Check your model number or UDI code against the list 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-2410-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2410-2025 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.
