EVA NEXUS Posterior 27G TDC PackRecalls & reported problems across all models
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one EVA NEXUS Posterior 27G TDC Pack model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of EVA NEXUS Posterior 27G TDC Pack by D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
EVA NEXUS Posterior 27G TDC Pack recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Apr 30, 2026Class IIOpen, Classified
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Z-2324-2026 · Root cause: Process design · names 2 of these models · Recall details · FDA record ↗
EVA NEXUS Posterior 27G TDC Pack models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- EVA NEXUS™ Posterior 27G TDC Pack 9311.27G01Instrument, Vitreous Aspiration And Cutting, Ac-Powered1 recall0 reports
- EVA NEXUS™ Posterior 27G TDC Pack 9311.27G01-00Instrument, Vitreous Aspiration And Cutting, Ac-Powered1 recall0 reports
Other D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. products
All D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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