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

Recall Z-1575-2025 — Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A Product Description: Influenza A And Influenza B Multiplex Nucleic Acid Assay; Real Time Nucleic Acid Component: No

U.S. FDA — Device Enforcement · United States · 2025-03-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1575-2025
Date of alert: 2025-03-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Abbott Diagnostics Scarborough, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10811877010422

Reported risk: the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.

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.

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.

Recall Z-1575-2025 — Brand Name: ID NOW Influenza A/B 2 24T Product Name: ID NOW Influenza A/B 2 24T Model/Catalog Number: 427-000 Software Version: N/A Product Description: Influenza A And Influenza B Multiplex Nucleic Acid Assay; Real Time Nucleic Acid Component: No

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