Vascular Probe 7452025Recalls & reported problems
Synovis Life Technologies, Inc. · The Vascular Probe is a sterile, single use, disposable polymeric device with a streamline bulb on each end of a flexible shaft. The bulbs are of different size on each end of the Vascular Probe. · Class 2
All models of Vascular Probe (9)
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.
2 other recalls cover devices cleared under the same FDA submission (K130896); 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
- 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 · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K130896. One submission often covers many models, so check the product and lot details in each record.
- Z-1524-2024 · Feb 22, 2024 · Open, ClassifiedSurgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-A
- Z-0659-2024 · Dec 6, 2023 · Open, ClassifiedBaxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.5-2 MM GLOBAL, c) 7082025: 8CM, 2-2.5 MM GLOBAL, d) 7151015: 15CM, 1-1.5 MM
Other DILATOR, VESSEL, SURGICAL devices
- Vascular Probe 7151015Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7451015ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7151520ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7451520ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7081520ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7151015ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe 7081520Synovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
- Vascular Probe Extra Supple 7152025ESSynovis Life Technologies, Inc. · DILATOR, VESSEL, SURGICAL1 recall0 reports
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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