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GE Healthcare recall records

24 reported ongoing

24 records in this archive. Latest source date Jul 31, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

FDA device enforcement

Universal Viewer Workflow Manager, Image processing radiological system

When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.

Class IIReported ongoing

Distribution: Nationwide distribution to AR, AZ, CA, CO, DE, FL, GA, IL, IN, ME, MI, MN, MO, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX. International distribution to Austria, Canada, Fra...

Official source
FDA device enforcement

Centricity PACS-IW with Universal Viewer, Model/Catalog Numbers: a) 2066908-061, b) 2066908-077, c) 2066908-086, d) 2066908-111, e) 2066908-123, f) 2066908-136, g) 2066908-150; ...

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

Class IIReported ongoing

Distribution: Worldwide Distribution

Official source
FDA device enforcement

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) 2088026-1...

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

Class IIReported ongoing

Distribution: Worldwide Distribution

Official source
FDA device enforcement

Centricity PACS-IW, Product ID Numbers: a) 2041037-001, b) 2042988-001, c) 2049587-009, d) 2049587-011, e) 2049587-012, f) 2049587-015, g) 2052829-001, h) Not applicable; Radiol...

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

Class IIReported ongoing

Distribution: Worldwide Distribution

Official source

Reasons in these listed records

  • When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.
  • GE HealthCare has become aware of an issue where information from two different patients can be mismatched when correcting patient or study information.

These examples come from this result page and are not a ranking of every recall reason.

Checking GE Healthcare

Is there a recall on ge healthcare right now?

This archive contains 24 records, including 24 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

Keep checking

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