Philips recalls XL14-3 transducers refurbished beyond useful life. Affected units may fail or cause injury. Contact Philips for details.
Ultrasound transducer devices were refurbished beyond their useful life.
Philips is recalling transducers that were refurbished beyond their intended lifespan. This could lead to failure or injury if used.
Refurbished transducers may not function properly after being reused. This could cause device failure or injury during medical procedures.
Users of Philips XL14-3 transducers with model number 989605409251 are affected. Most at risk are medical professionals using these devices.
Check for model number 989605409251 on the transducer. The UDI code (01)00884838074613(21)B1ZL08 and serial number B1ZL08 are also indicators.
Look for model number 989605409251 on the transducer.
The transducers were refurbished beyond their useful life, which could lead to failure or injury.
Check for model number 989605409251, UDI code (01)00884838074613(21)B1ZL08, and serial number B1ZL08.
The recall does not specify a remedy, so contact Philips directly for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2068-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2068-2025 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.
