# FDA recall Z-1501-2023

> **GE Healthcare** · Class II · device recall initiated 2023-03-28.

## Product

Centricity Universal Viewer, Centricity Universal Viewer 6.0,  Model/Catalog Numbers:   a) 2088026-003,  b) 2088026-026,  c) 2088026-032,  d) 2088026-043,  e) 2088026-044,  f) 2088026-115,  g) 2088026-132,  h) 2088026-306,  i) 2088026-308,  j) 2088026-406,  k) 2088026-506,  l) 2088026-613,  m) 2088026-713,  n) 2088026-714,  o) 2088026-723,  p) 2099714-001,  q) 2100169-001,  r) 2100491-006,  s) 2102675-010,  t) 2102676-001,  u) 2104867-044,  v) 2104867-045;   Radiological Image Processing System

## Reason for recall

GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.

## Distribution

Worldwide Distribution

## Key facts

- **Recall number:** Z-1501-2023
- **Recalling firm:** GE Healthcare
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-28
- **Report date:** 2023-05-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1501-2023

## Citation

> AI Analytics. FDA recall Z-1501-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1501-2023. Source: US FDA. Licensed CC0.

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