Abbott Molecular, Inc. recalls

5 recalls on record · latest: April 28, 2025

Official U.S. recall history for Abbott Molecular, Inc., compiled from official government records.

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Abbott Molecular, Inc. recalls Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription…

April 28, 2025 · Medical device recalls Moderate risk There were reports of an increase in reactive negative controls and false posit…

Abbott Molecular, Inc. recalls Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain…

April 28, 2025 · Medical device recalls Moderate risk There were reports of an increase in reactive negative controls and false posit…

Abbott Molecular, Inc. recalls The Alinity m System is designed to automate the steps for nucleic acid testing. Model Numbers included in this recall…

March 20, 2025 · Medical device recalls Moderate risk The design of the Alinity m System Solutions drawer enclosure may allow liquid…

Abbott Molecular, Inc. recalls Abbott Alinity m STI AMP Kit, used with the Alinity m System, product codes: a) REF 09N17-095; b) REF 09N17-090; c) REF…

September 12, 2024 · Medical device recalls Moderate risk Abbott has identified an increase of incidences regarding Error Code (EC) 9198…

Abbott Molecular, Inc. recalls Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…

September 12, 2024 · Medical device recalls Moderate risk Abbott has identified an increase of incidences regarding Error Code (EC) 9198…