A.i.d.d Longford
FDA adverse event reports naming A.i.d.d Longford as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: A.I.D.D LONGFORD.
- Total reports
- 2,027
- Deaths
- 1
- Injuries
- 32
- Malfunctions
- 1,994
Reports per year
409
1910
17811
6812
6313
11814
2815
5616
8117
28618
37719
10720
25921
31022
7323
Source: FDA adverse event reports by year received, 2009–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Test, Human Chorionic GonadotropinDHA787
- Radioimmunoassay, Total TriiodothyronineCDP517
- Immunoassay Method, Troponin SubunitMMI270
- Radioimmunoassay, Thyroid-Stimulating HormoneJLW264
- Radioimmunoassay, Prolactin (Lactogen)CFT67
- Radioimmunoassay, EstradiolCHP38
- Radioassay, Vitamin B12CDD30
- Photometric Method, MagnesiumJGJ28
- System, Identification, Hepatitis B AntigenKSJ8
- Ferritin, Antigen, Antiserum, ControlDBF7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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