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Phadia US Inc
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Type Company Card addedAugust 10 Threat lists flagged Reviews1
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Threat lists · flagged Product safety recall
Official safety regulators published alerts about a product of this kind.
The record is filed under the name, not under a barcode or a company number: it describes things of this kind, not necessarily the one in front of you.
Alerts on record2 HazardHigher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument First alertMay 1, 2023 Latest alertMay 1, 2023 On our lists sinceAugust 10, 2026
What to do: Check the maker, the batch and the date of the exact item you have — the alert is about this kind of product.
Where this came from: openFDA device recalls — An official government safety register — product recalls and safety alerts.
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Reviews · 1
Phadia US Inc belongs to allergy and immunology diagnostics, where blood tests and laboratory instruments help identify sensitizations and related conditions. By our assessment, this is a technical healthcare company for labs and clinicians, not a patient-facing brand, and its strength is in specialized testing rather than broad recognition. The trade-off is that such products can feel opaque unless you work around them, because the value sits in assay design, workflow, and interpretation. In practice, that means careful sample handling, instrument support, and a lot of dependence on the lab environment itself. Phadia US Inc sits in a narrower, more specialized slice of diagnostics than general lab suppliers, which makes it useful but not universal. It is a good fit where allergy testing is routine, and outside that lane the appeal falls away quickly.
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