FDA recall record

RAYSEARCH LABORATORIES AB RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology recall — FDA Z-1281-2021

Patient related messages created in RayCare 3B, RayCare 4A will be lost when upgrading from RayCare 2 to RayCare 3B or later

Class IIclassification
Z-1281-2021official record ID
Mar 31, 2021report date

Recall record at a glance

Official recordZ-1281-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRAYSEARCH LABORATORIES AB
Report dateMar 31, 2021
Recall initiation dateMar 3, 2021
Quantity1 unit
LocationStockholm, N/A, Sweden

Official product description

RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information system that supports healthcare professionals in delivering cancer care.

Why the product was recalled

Patient related messages created in RayCare 3B, RayCare 4A will be lost when upgrading from RayCare 2 to RayCare 3B or later

Distribution information

US Nationwide distribution in the state of TN.

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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