L8-4 Transducer Probe
Reported: September 3, 2025 Initiated: July 3, 2025 #Z-2381-2025
Product Description
L8-4 Transducer Probe
Reason for Recall
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Details
- Recalling Firm
- Philips Ultrasound, Inc
- Units Affected
- 171,322 units
- Distribution
- US Nationwide distribution.
- Location
- Reedsville, PA
Frequently Asked Questions
What product was recalled? ▼
L8-4 Transducer Probe. Recalled by Philips Ultrasound, Inc. Units affected: 171,322 units.
Why was this product recalled? ▼
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 3, 2025. Severity: Low. Recall number: Z-2381-2025.
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