Philips recalls S7-2t Transducer Probes with specific model numbers for labeling clarity on useful life in medical ultrasound field use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain S7-2t Transducer Probes to clarify labeling for the useful life of these ultrasound probes in medical field use. This recall does not involve safety hazards but aims to improve labeling for product longevity.
The recall focuses on providing clearer labeling for the useful life of the transducers in medical field use. There is no safety hazard described; this is a labeling clarification to help users understand product longevity.
Medical professionals using Philips S7-2t Transducer Probes with the listed model numbers are likely affected. Patients using these probes for ultrasound imaging may also be impacted by the labeling clarification.
Check for model numbers 21778A, 989605440772, or UDI codes starting with (01)00884838067646(21) followed by specific alphanumeric sequences listed in the recall. Serial numbers like B04LH4, B199HC, etc., are also part of the affected units.
Look for model numbers 21778A, 989605440772, or UDI codes starting with (01)00884838067646(21) followed by specific alphanumeric sequences listed in the recall.
Philips is recalling these transducers to provide clearer labeling for the useful life in medical field use, not due to a safety hazard.
No, this recall does not require stopping use; it's for labeling clarification to help users understand product longevity.
Check the product label for model numbers or UDI codes listed in the recall to confirm if it's affected. No action is needed beyond checking the label.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2396-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2396-2025 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.
