Multi-TrackRecalls & reported problems across all models

We found 2 models of Multi-Track by B Braun Interventional Systems, 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.

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

Multi-Track 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. Oct 17, 2018Terminated

   Instructions for Use booklets were not included on the outer pouch

   Z-0511-2019 · Root cause: Labeling design · Recall details · FDA record ↗

2. Oct 17, 2018Terminated

   Instructions for Use booklets were not included on the outer pouch

   Z-0510-2019 · Root cause: Labeling design · Recall details · FDA record ↗

Multi-Track models

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

• Multi-Track™ 615001

  CATHETER, INTRAVASCULAR, DIAGNOSTIC
  1 recall0 reports
• Multi-Track™ 615009

  CATHETER, INTRAVASCULAR, DIAGNOSTIC
  1 recall0 reports

Other B Braun Interventional Systems, Inc products

• CELSITE7 models · 17 reports · 1 recall
• BIB6 models · 5 reports · 1 recall
• VENA TECH2 models · 48 reports
• CP Stent16 models · 29 reports
• TYSHAK II12 models · 25 reports