Philips Ultrasound recalls D5cwc Transducer Probes with specific model numbers for labeling clarification to define useful life in field use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound is recalling certain D5cwc Transducer Probes to clarify labeling and define their useful life in field use. This recall does not involve safety hazards but aims to improve product labeling.
The recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard or risk of injury described.
Users of Philips D5cwc Transducer Probes with the listed model numbers are affected. Medical professionals using ultrasound equipment are most at risk.
Check your D5cwc Transducer Probe for model numbers 989605438561 or 989605412062. Also look for UDI codes starting with (01)00884838061354(21) followed by specific alphanumeric sequences listed in the recall.
Look for model numbers 989605438561 or 989605412062 on your D5cwc Transducer Probe.
Check the Unique Device Identification (UDI) code on the product, which starts with (01)00884838061354(21) followed by specific alphanumeric sequences listed in the recall.
No, this recall is for labeling clarification to define the useful life of ultrasound transducers in the field. There is no safety hazard described.
Check your D5cwc Transducer Probe for model numbers 989605438561 or 989605: 989605412062. If you have the listed model numbers, you should check the UDI code to confirm if your product is affected.
Look for model numbers 989605438561 or 989605412062 on your D5cwc Transducer Probe. Also check the UDI code starting with (01)00884838061354(21) followed by specific alphanumeric sequences listed in the recall.
We’ve drafted a message you can send Philips Ultrasound to request your refund or repair — edit it as you like.
Subject: Recall Z-2368-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2368-2025 from Philips Ultrasound. 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.
