Merit KitRecalls & reported problems across all models

We found 2 models of Merit Kit by Merit Medical 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

Merit Kit 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. Sep 20, 2017Terminated

   1 Cuff catheters were incorrectly configured and labeled as 2 Cuff product and placed into these dialysis kits.

   Z-1145-2018 · Root cause: Mixed-up of materials/components · Recall details · FDA record ↗

2. Sep 20, 2017Terminated

   2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product and placed into these dialysis kits.

   Z-1144-2018 · Root cause: Mixed-up of materials/components · Recall details · FDA record ↗

Merit Kit models

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

• Merit® Kit 00884450328613

  Dialysis administration kit
  1 recall0 reports
• Merit® Kit 00884450328620

  Dialysis administration kit
  1 recall0 reports

Other Merit Medical Systems, Inc. products

• Aspira11 models · 36 reports · 10 recalls
• Impress145 models · 481 reports
• Monarch6 models · 37 reports · 7 recalls
• Bridge Prep Kit4 models · 6 reports · 3 recalls
• Prelude Roadster33 models · 1 reports · 3 recalls
• basixTOUCH6 models · 1 reports · 3 recalls
• basixCOMPAK34 models · 34 reports · 2 recalls
• Flex-Neck11 models · 21 reports · 2 recalls