FDA recall record

Change Healthcare Enterprise Viewer recall — FDA Z-1508-2021

Change Healthcare has identified an intermittent software defect which may result in an anchor study failing to display.

Class IIclassification
Z-1508-2021official record ID
May 5, 2021report date

Recall record at a glance

Official recordZ-1508-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCHANGE HEALTHCARE CANADA COMPANY
Report dateMay 5, 2021
Recall initiation dateMar 17, 2021
Quantity28 units
LocationRichmond, N/A, Canada

Official product description

Change Healthcare Enterprise Viewer

Why the product was recalled

Change Healthcare has identified an intermittent software defect which may result in an anchor study failing to display.

Distribution information

Domestic Distribution only. IN, KY, CA, NY, WA, IL, IA, FL, TX, WA, MI, HI, AK, WI, WY, NE, AZ, OH, PA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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