YelloPort Elite EO0507005Recalls & reported problems
Surgical Innovations Limited · 5x70 Optical Trocar · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
1 other recall cover devices cleared under the same FDA submission (K210495); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Mar 28, 2023Open, Classified
Optical Trocars sterility assurance can not be guaranteed
Z-1601-2023 · Root cause: Other · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K210495. One submission often covers many models, so check the product and lot details in each record.
- Z-1602-2023 · Mar 28, 2023 · Open, ClassifiedYelloPort Elite, REF: EO0509505, 5x95 Optical Trocar, Rx Only, SterileR
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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