CORMIXRecalls & reported problems across all models

We found 4 models of CORMIX by Metrix Company, The in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Jun 18, 2021 and Mar 28, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (1 report).

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

CORMIX 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 9, 2024Open, Classified

   A limited number of IV bags have been found to leak during filling.

   Z-0334-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

2. Oct 9, 2024Open, Classified

   A limited number of IV bags have been found to leak during filling.

   Z-0333-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

3. Oct 9, 2024Open, Classified

   A limited number of IV bags have been found to leak during filling.

   Z-0332-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported CORMIX problems

CORMIX models

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

• CORMIX MS64045

  Container, I.V.
  1 recall1 report
• CORMIX MS64040

  Container, I.V.
  1 recall0 reports
• CORMIX MS64050

  Container, I.V.
  1 recall0 reports
• CORMIX MS64230

  Container, I.V.
  1 report

Recent CORMIX adverse event reports

The 2 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMar 28, 2024Contamination /Decontamination Problem; Contamination /Decontamination Problem

  CUSTOMER FOUND "PLASTIC FLOATING IN THE BAG AFTER MIXING A TPN" DURING INSPECTION OF THE PRODUCT BY A HEALTHCARE PROVIDER. THE PRODUCT WAS NOT BEING ADMINISTERED, AND THERE WAS NO PATIENT INVOLVEMENT. THE SAMPLE WAS NOT AVAILABLE FOR EVALUATION. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18996047 ↗
• MalfunctionJun 18, 2021Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT WHILE COMPOUNDING MILRINONE AND D5W INTO A CORMIX EMPTY EVA CONTAINER WITH 2 PORTS, THAT AN OBJECT WITH THE APPEARANCE OF LEGS AND A WING WERE VISIBLE INSIDE THE BAG. IT WAS FURTHER REPORTED THAT THE COMPOUNDING TECHNICIAN CUT THE BAG AND EXTRACTED IT FROM INSIDE USING A NEEDLE TO CONFIRM THAT IT WAS NOT CORING. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12027225 ↗

Other Metrix Company, The products

• SECURE16 models · 43 reports · 8 recalls