Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122
Reported: January 7, 2026 Initiated: July 14, 2022 #Z-1007-2026
Product Description
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122
Reason for Recall
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Details
- Recalling Firm
- Philips Ultrasound, LLC
- Units Affected
- 1,721 systems
- Distribution
- Worldwide - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of Argentina, Australia, Belgium, Canada, Chile, Colombia, Czech Republic, Denmark, Ecuador, Estonia, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Iran, Iraq, Ireland, Israel, Italy, Japan, Korea, Republic of Latvia, Lithuania, Morocco, Netherlands , New Zealand, Oman, Panama, Philippines, Poland, Romania, Russian Federation, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, United Kingdom.
- Location
- Bothell, WA
Frequently Asked Questions
What product was recalled? ▼
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122. Recalled by Philips Ultrasound, LLC. Units affected: 1,721 systems.
Why was this product recalled? ▼
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 7, 2026. Severity: Moderate. Recall number: Z-1007-2026.
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