FDA recall record

Phadia Ab EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000 recall — FDA Z-0783-2024

Complaints that specific samples produced false positive EliA GBM results. A positive signal was present when these samples were tested for…

Class IIclassification
Z-0783-2024official record ID
Jan 31, 2024report date

Recall record at a glance

Official recordZ-0783-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmPhadia Ab
Report dateJan 31, 2024
Recall initiation dateMay 24, 2023
Quantity124,928 kits
LocationUppsala, N/A, Sweden

Official product description

EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic

Why the product was recalled

Complaints that specific samples produced false positive EliA GBM results. A positive signal was present when these samples were tested for coating-solution reactivity using EliA wells without antigen.

Distribution information

US 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: 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

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