Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
Reported: July 24, 2019 Initiated: July 2, 2019 #Z-1964-2019
Product Description
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D
Reason for Recall
Potential for a transducer mis-alignment in certain transvaginal probes.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- 3 devices
- Distribution
- Distribution in the US to Texas. International distribution to France, Greece and Switzerland.
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D. Recalled by GE Healthcare, LLC. Units affected: 3 devices.
Why was this product recalled? ▼
Potential for a transducer mis-alignment in certain transvaginal probes.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 24, 2019. Severity: Moderate. Recall number: Z-1964-2019.
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