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Bioporto Diagnostics recalls

Bioporto Diagnostics has 1 recall on record with the FDA and USDA, the earliest in 2026 and the latest reported on 19 Aug 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls1since 2026

Last 12 months1reported

Class I00% of total

Ongoing1latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 1 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why bioporto diagnostics is recalled

Potency & Assay1100%

Product types

Test Kits & Diagnostics1100%

By year

20261100%

Ongoing bioporto diagnostics recalls

1 active

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	ProNephro AKI (NGAL) Reagent Kit (100 tests) recalled	Bioporto Diagnostics	Potency & Assay

All bioporto diagnostics recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
19 Aug 2026Device	CLASS II	ProNephro AKI (NGAL) Reagent Kit (100 tests) recalled	Bioporto Diagnostics	Potency & Assay

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.