Abbott Diagnostics Scarborough, Inc.: Device Recall

Recall #Z-1575-2025 · 03/04/2025

Class II: Risk

Recall Details

Recall Number
Z-1575-2025
Classification
Class II
Product Type
Device
Recalling Firm
Abbott Diagnostics Scarborough, Inc.
Status
Ongoing
Date Initiated
03/04/2025
Location
Scarborough, ME, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
2,776,416 eaches

Reason for Recall

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

Product Description

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

Distribution Pattern

US Nationwide distribution.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.