Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2927-2026 — Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics

U.S. FDA — Device Enforcement · United Kingdom · 2026-07-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2927-2026
Date of alert
2026-07-17
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
Remel Europe Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05056080501161
Reported risk: Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.