FDA recall record

Best Theratronics cabinet x-ray systems intended for use in the irradiation of blood and recall — FDA Z-2251-2016

It was discovered that both the new device and the predicate device failed to comply with performance standard.

Class IIclassification
Z-2251-2016official record ID
Aug 3, 2016report date

Recall record at a glance

Official recordZ-2251-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBEST THERATRONICS LTD.
Report dateAug 3, 2016
Recall initiation dateMay 6, 2016
Quantity128
LocationKANATA, N/A, Canada

Official product description

Best Theratronics cabinet x-ray systems intended for use in the irradiation of blood and blood products (packaged in transfusion bags) to inactivate T-lymphocytes for the prevention of Graft Versus Host Disease.

Why the product was recalled

It was discovered that both the new device and the predicate device failed to comply with performance standard.

Distribution information

Nationwide

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: FDA Mandated. 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

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