# FDA recall Z-0864-2021

> **Philips Ultrasound Inc** · Class II · device recall initiated 2020-10-27.

## Product

All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ CVx, Affiniti 30, Affiniti 50, Affiniti 70. Diagnostic Ultrasound System.     MOD - EPIQ 5 GMDN - 40761 100-240V 50/60 Hz, 600 VA  MOD - EPIQ 7 GMDN - 40761 100-240V 50/60 Hz, 600 VA  MOD - EPIQ 100-240V 50/60 Hz, 600 VA  MOD - Affinity 30 GMDN - 40761 100-240V 50/60 Hz, 450 VA  MOD - Affinity 50 GMDN - 40761 100-240V 50/60 Hz, 450 VA  MOD - Affinity 70 GMDN - 40761 100-240V 50/60 Hz, 450 VA

## Reason for recall

The manufacturer has determined that with certain uncommon workflows there is potential for incorrect patient data to be displayed and saved into an exam. The issue(s) manifest differently for different versions of software.

## Distribution

Worldwide distribution - US Nationwide distribution including 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, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY. The countries of  Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bermuda, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Canada, Chile, China, Colombia, Cook Islands, Costa Rica, Corte D'Ivoire, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Estonia, Ethiopia, Faroe Islands, Finland, France, French Guiana, French Polynesia, Georgia, Germany, Ghana, Gibraltar, Greece, Greenland, Guadeloupe, Guatemala, Guernsey, Honduras, Hong Kong, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kuwa

## Key facts

- **Recall number:** Z-0864-2021
- **Recalling firm:** Philips Ultrasound Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-10-27
- **Report date:** 2021-01-20
- **Termination date:** 2023-04-19

- **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-0864-2021

## Citation

> AI Analytics. FDA recall Z-0864-2021. Retrieved 2026-09-09 from https://api.ai-analytics.org/recall/Z-0864-2021. Source: US FDA. Licensed CC0.

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