Immucor, Inc.
FDA adverse event reports naming Immucor, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: IMMUCOR, INC..
- Total reports
- 3,265
- Deaths
- 0
- Injuries
- 8
- Malfunctions
- 3,230
Reports per year
23312
22113
24014
22715
32716
34017
28418
14919
6020
3021
1922
2723
2124
2825
1026
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Test, Automated Blood Grouping And AntibodyKSZ3,069
- Kit, Quality Control For Blood Banking ReagentsKSF68
- Reagent Red Blood CellsQHT60
- Supplies, Blood-BankKSS15
- Blood Grouping ReagentQHR10
- Product code MWNMWN9
- Antigens, Nontreponemal, AllGMQ6
- Antibody Igm,If, Cytomegalovirus VirusLKQ6
- Antigen, Iha, CytomegalovirusLJO5
- Blood Establishment Computer Software And AccessoriesMMH3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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