BD Vacutainer PST Blood Collection TubesRecalls & reported problems across all models

We found 2 models of BD Vacutainer PST Blood Collection Tubes by Becton, Dickinson And Company 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

BD Vacutainer PST Blood Collection Tubes 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. Jun 12, 2019Class IITerminated

   False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.

   Z-2308-2019 · Root cause: Device Design · Recall details · FDA record ↗

2. Jun 12, 2019Class IITerminated

   False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.

   Z-2306-2019 · Root cause: Device Design · names 2 of these models · Recall details · FDA record ↗

BD Vacutainer PST Blood Collection Tubes models

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

• BD Vacutainer® PST™ Blood Collection Tubes 368035

  Tubes, vials, systems, serum separators, blood collection
  2 recalls0 reports
• BD Vacutainer® PST™ Blood Collection Tubes 368036

  Tubes, vials, systems, serum separators, blood collection
  1 recall0 reports

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