Mallinckrodt Medical
FDA adverse event reports naming Mallinckrodt Medical as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MALLINCKRODT MEDICAL.
- Total reports
- 2,744
- Deaths
- 23
- Injuries
- 306
- Malfunctions
- 2,376
Reports per year
1605
906
507
114
115
20817
13218
17619
8220
12521
19122
24723
27224
46625
22926
Source: FDA adverse event reports by year received, 2005–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Tube Tracheostomy And Tube CuffJOH1,088
- Tube, Bronchial (W/Wo Connector)BTS861
- Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)CBI358
- Tube, Tracheal (W/Wo Connector)BTR338
- Tube, Tracheostomy (W/Wo Connector)BTO40
- Attachment, Breathing, Positive End Expiratory PressureBYE16
- Airway, Oropharyngeal, AnesthesiologyCAE8
- Catheter, Intravascular, DiagnosticDQO5
- Wire, Guide, CatheterDQX5
- Cuff, Tracheal Tube, InflatableBSK3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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