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

Recall Z-1740-2022 — Helix Elite Inactivated Standard, labeled as: a. Inactivated SARS-CoV-2 B.1.1.7 Whole Virus, REF HE0071N; b. Inactivated SARS-CoV-2 B.1.351 Whole Virus, REF HE0073N

U.S. FDA — Device Enforcement · United States · 2022-07-27 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1740-2022
Date of alert
2022-07-27
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Microbiologics Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10845357043846
Reported risk: Product not registered for use in the UK
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.