Becton Dickinson DE Mexico
FDA adverse event reports naming Becton Dickinson DE Mexico as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON DE MEXICO.
- Total reports
- 1,213
- Deaths
- 0
- Injuries
- 16
- Malfunctions
- 1,197
Reports per year
100
103
104
116
1317
9818
20719
19320
14821
12822
14723
9024
13125
5426
Source: FDA adverse event reports by year received, 2000–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Syringe, PistonFMF1,082
- Needle, Hypodermic, Single LumenFMI89
- Needle, Aspiration And Injection, DisposableGAA10
- Culture Media, Non-Selective And Non-DifferentialJSG7
- Culture Media, Selective And Non-DifferentialJSJ6
- Culture Media, Non-Selective And DifferentialJSH5
- Culture Media, Selective And DifferentialJSI3
- Needle, DentalDZM2
- Saline, Vascular Access FlushNGT2
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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