FDA recall record

Merge Healthcare DR Systems Unity PACS software, now known as Merge Unity PACS recall — FDA Z-1426-2017

Reports were missing demographic header information when they were faxed to referring physicians.

Class IIclassification
Z-1426-2017official record ID
Mar 15, 2017report date

Recall record at a glance

Official recordZ-1426-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMerge Healthcare, Inc.
Report dateMar 15, 2017
Recall initiation dateApr 8, 2016
Quantity9 sites potentially have the affected version
LocationHartland, WI, United States

Official product description

DR Systems Unity PACS software, now known as Merge Unity PACS

Why the product was recalled

Reports were missing demographic header information when they were faxed to referring physicians.

Distribution information

US Distribution was made to medical facilities in CA, MT, PA, and TX. There was no foreign/military/government distribution.

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: E-Mail.

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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