Flo-Rester Disposable Internal Vessel OccluderRecalls & reported problems across all models

We found 24 models of Flo-Rester Disposable Internal Vessel Occluder 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.

3 FDA recall records name at least one of these models by its device identifier, 3 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

Flo-Rester Disposable Internal Vessel Occluder 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.

1. Feb 22, 2024Class IIOpen, 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 10 of these models · Recall details · FDA record ↗

2. Feb 22, 2024Class IIOpen, 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-1523-2024 · Root cause: Under Investigation by firm · names 9 of these models · Recall details · FDA record ↗

3. Feb 22, 2024Class IIOpen, 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 ↗

Flo-Rester Disposable Internal Vessel Occluder models

24 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Flo-Rester® Disposable Internal Vessel Occluder 50100

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50125

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50150

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50175

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50200

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50225

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50250

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50275

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50300

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50350

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50400

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 50450

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60100

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60125

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60150

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60175

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60200

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60225

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60250

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60275

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60300

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60350

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60400

  CLAMP, VASCULAR
  1 recall0 reports
• Flo-Rester® Disposable Internal Vessel Occluder 60450

  CLAMP, VASCULAR
  1 recall0 reports

Other Synovis Life Technologies, Inc. products

• Peri-Guard10 models · 2 reports · 2 recalls
• Vascular Probe9 models · 0 reports · 2 recalls
• Vascular Probe Extra Supple9 models · 0 reports · 2 recalls
• Supple Peri-Guard9 models · 0 reports · 2 recalls
• Flo-Thru Intraluminal Shunt9 models · 2 reports · 1 recall