# FDA recall Z-1007-2026

> **Philips Ultrasound, LLC** · Class II · device recall initiated 2022-07-14.

## Product

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.

## 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.

## Key facts

- **Recall number:** Z-1007-2026
- **Recalling firm:** Philips Ultrasound, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2022-07-14
- **Report date:** 2026-01-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bothell, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1007-2026

## Citation

> AI Analytics. FDA recall Z-1007-2026. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-1007-2026. Source: US FDA. Licensed CC0.

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