Abbott Molecular, Inc.: Medical Device Recalls in 2022
Updated on March 25, 2026.
According to to data from the FDA, there were 12 medical device recalls made by Abbott Molecular, Inc. in 2022. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Alinity m Integrated Reaction Units (IRU)
- Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-096
- Alinity m HBV Application Specification File (US and CE)
- The Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use.
- Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-090
- Alinity m HBV AMP Kit (US and CE)
- Alinity m System, Part No. 08N53-002
- Alinity m System, Part No. 08N53-002
- Alinity m System, Part No. 08N53-002
- Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In Vitro Diagnostic Use.
- Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use
- Alinity m System, Part No. 08N53-002