Vascular ProbeRecalls & reported problems across all models
Synovis Life Technologies, Inc. · 9 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one Vascular Probe 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
- 2
We found 9 models of Vascular Probe by Synovis Life Technologies, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
2 FDA recall records name at least one of these models by its device identifier, 2 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
Vascular Probe 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.
- Feb 22, 2024Open, Classified
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Z-1524-2024 · Root cause: Under Investigation by firm · names 4 of these models · Recall details · FDA record ↗
- Feb 22, 2024Open, Classified
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Z-1522-2024 · Root cause: Under Investigation by firm · names 5 of these models · Recall details · FDA record ↗
Vascular Probe models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Vascular Probe 7081015DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7081520DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7082025DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7151015DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7151520DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7152025DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7451015DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7451520DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7452025DILATOR, VESSEL, SURGICAL1 recall0 reports
Other Synovis Life Technologies, Inc. products
All Synovis Life Technologies, Inc. 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page