Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott Diagnostics Scarborough, Inc. Due to The impacted lots have a higher occurrence of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Abbott Diagnostics Scarborough, Inc. directly.
Affected Products
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No
Quantity: 339456 eaches (337560 US, 1896 OUS)
Why Was This Recalled?
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Abbott Diagnostics Scarborough, Inc.
Abbott Diagnostics Scarborough, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report