VDW Gmbh
FDA adverse event reports naming VDW Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: VDW GMBH.
- Total reports
- 1,123
- Deaths
- 0
- Injuries
- 37
- Malfunctions
- 1,086
Reports per year
104
112
119
1520
3521
25222
19823
22724
18425
20926
Source: FDA adverse event reports by year received, 2004–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- File, Pulp Canal, EndodonticEKS595
- Locator, Root ApexLQY205
- Handpiece, Contra- And Right-Angle Attachment, DentalEGS175
- Syringe, Periodontic, Endodontic, IrrigatingEIC98
- Controller, Foot, Handpiece And CordEBW45
- Reamer, Pulp Canal, EndodonticEKP2
- Instrument, Filling, Plastic, DentalEIY1
- Gutta-PerchaEKM1
- Plugger, Root Canal, EndodonticEKR1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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