Reported Apr 23, 2025 · Ongoing
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software…
Abbott Diagnostics Scarborough, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Abbott Diagnostics Scarborough, Inc. · 10 Southgate Rd · Scarborough, ME · 04074-8303
Is this the product you have?
- Brand NameID NOW COVID-19 2.0 24T
- Product NameID NOW COVID-19 2.0 24T
- Model/Catalog Number192-000
- Software VersionN/A
- Product DescriptionSimple Point-Of-Care Device To Detect Sar-Cov-2
- Nucleic Acid Targets ComponentNo
- Lot codes and dates
59 of 59 products
Products covered by this recall Model / number Barcodes Product as published 192-000— — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M884910 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M885121 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M911157 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M913227 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M913286 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M913303 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M913641 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M914188 — 10811877011351GTIN/DI 10811877011351 192-000Lot 000M914221 — 10811877011351GTIN/DI 10811877011351 - Amount recalled
- 2,164,872 eaches
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
This product could cause temporary or reversible health problems — stop using it.
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