Philips recalls specific models of OMNI III TEE Ultrasound Transducers for labeling clarification to define useful life in field use. No action required for safety, but updated labeling helps with product lifecycle management.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain OMNI III TEE Ultrasound Transducers to clarify their useful life labeling in field use. This recall does not pose a safety risk but aims to provide better information for proper product management.
The recall addresses labeling clarification for the useful life of the transducers in clinical use. This ensures accurate information about how long the device can be safely used before needing replacement or recalibration.
Medical professionals using Philips OMNI III TEE Ultrasound Transducers with the listed model numbers and serial codes. Patients using these devices are not at risk.
Check for model numbers 989605440701, 989605440702, 989605440772, or 989803001561. Also look for serial numbers like 02ZTTT, 02DFBP, B0X7MD, or 039MMD.
Check the device label for model numbers and serial codes to confirm if it is part of the recalled batch.
No, this recall is for labeling clarification to define the useful life of the transducers in field use. It does not pose a safety risk.
No action is required for safety. The recall is informational and does not affect device safety.
Check the model numbers (989605440701, 989605440702, 989605440772, 989803001561) and serial numbers (e.g., 02ZTTT, 02DFBP) on the device label.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1624-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1624-2026 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.
