RecallReported September 23, 2026
Class II recall by GE Healthcare
Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administ…
FDA's enforcement report of September 23, 2026 lists a Class II recall by GE Healthcare of Chicago, IL. Product: Workflow Core Services V8, intended to provide set of services for storage and retrieval of patient data, exams and performs system Administ…. Status: Ongoing.
On the record
- Recalling firm
- GE Healthcare
- Location
- Chicago, IL
- Classification
- Class II
- Status
- Ongoing
- Recall number
- Z-3170-2026
- Product type
- Devices
- Recall initiated
- 2026-07-31
- Reported by FDA
- 2026-09-23
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
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From FDA enforcement reports. The record may have changed since it was read.
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