Reported Dec 28, 2022 · Ongoing

Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-096

Abbott Molecular, 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 Molecular, Inc. · 1300 E Touhy Ave · Des Plaines, IL · 60018-3315

Is this the product you have?

    • Abbott Alinity m Resp-4-Plex Amp Kit
    • Part Number 09N79-096
Lot codes and dates
  • Lot Numbers
    • 381465
    • exp 8/24/2023
    • 524433
    • exp 1/5/2023
    • 526710
    • exp 1/21/2023
    • 527845
    • exp 2/8/20231499
Amount recalled
3896 kits

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Why it was recalled

Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:32 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.