Remel Europe recalls

2 recent recalls on record for Remel Europe in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

Oxoid Agglutinating Sera (1)Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL (1)

All Remel Europe recalls

FDA Class II · Medical device · August 19, 2026

Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL recall — Remel Europe Ltd.

Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.

Official ID Z-2927-2026 · Official record ↗

FDA Class II · Medical device · April 29, 2026

Oxoid Agglutinating Sera recall — Remel Europe Ltd.

Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O seroty…

Official ID Z-1923-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.