Philips Ultrasound recalls specific V6-2 Transducer Probes with model numbers 989605415042, 989605437982, and other serial numbers for labeling clarification on useful life in medical use.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound is recalling certain V6-2 Transducer Probes to clarify their useful life in medical settings. This is a labeling update, not a safety hazard.
The recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard or risk of injury.
Medical professionals using Philips V6-2 Transducer Probes with specific model and serial numbers listed in the recall. These are ultrasound devices for medical imaging.
Check your V6-2 Transducer Probe for model numbers 989605415042, 989605437982, or other serial numbers listed in the recall. The recall includes specific UDI codes and model numbers.
Review your V6-2 Transducer Probe for model numbers and UDI codes listed in the recall to determine if it is affected.
No, this recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard.
No action is required. This is a labeling update for useful life clarification, not a safety issue.
Affected models include 989605415042, 989605437982, and other specific model numbers and UDI codes 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-2403-2025 — Philips Ultrasound Philips Ultrasound Hello, I own a Philips Ultrasound that is covered by recall Z-2403-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.