BodyGuard Microset with FilterRecalls & reported problems across all models

We found 2 models of BodyGuard Microset with Filter by Cme America LLC in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.

1 FDA recall record 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

BodyGuard Microset with Filter 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. Jan 14, 2020Class IITerminated

   The filter installed onto the tube set may have the incorrect pore size.

   Z-1886-2020 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗

BodyGuard Microset with Filter models

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

• BodyGuard® Microset with Filter A120-112XSFK

  Set, Administration, Intravascular
  1 recall0 reports
• BodyGuard® Microset with Filter A120-160XSFK

  Set, Administration, Intravascular
  1 recall0 reports