Philips recalls specific C6-3 Transducer Probes for labeling clarification to define useful life in field use. No immediate safety risk but requires updated labeling for proper maintenance.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain C6-3 Transducer Probes to update labeling for field use duration. This helps users understand when the probe should be replaced based on usage. There is no safety risk involved in normal use.
The recall is for labeling clarification to define the useful life of the transducers in field use. This ensures users know when the probe should be replaced based on usage, preventing potential confusion about maintenance intervals.
Users of Philips C6-3 Transducer Probes with the listed model numbers and serial codes are affected. Healthcare professionals using these probes for ultrasound imaging are most at risk of confusion about replacement timelines.
Check for model numbers 989605359593, 989605387371, 989605359594, or 989605359591 on the probe. Also look for serial numbers like B20N4N, B1WR9H, or B1RGN0 on the device.
Check the probe's labeling for updated useful life instructions to ensure proper maintenance.
No, this recall is for labeling clarification to define the useful life of the transducers in field use. There is no safety risk.
Check for model numbers 989605359593, 989605387371, 989605359594, or 989605359591, or serial numbers like B20N4N, B1WR9H, or B1RGN0.
No, the recall does not require stopping use. The labeling update helps with proper maintenance timing.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2356-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2356-2025 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.
