Magic3 Go Pediatric Catheter with SureGrip 52806GRecalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00801741136856), received between Apr 4, 2019 and Jun 23, 2025 — classified as 9 malfunctions.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 23, 2025Component Misassembled; Component Misassembled

  IT WAS REPORTED THAT ONE OF THE CATHETERS WERE IN A KNOT AND THE OTHER ONE WAS BROKEN IN HALF. PER CUSTOMER VIA PHONE ON 11JUN2025, IT WAS REPORTED THAT SOME OF THE CATHETERS HAD NO HOLES AT THE END, SOME WERE BROKEN, AND SOME WERE TWISTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22307114 ↗
• MalfunctionMay 16, 2025Material Fragmentation; Material Fragmentation

  IT WAS REPORTED THAT ONE OF THE INTERMITTENT CATHETERS WERE IN A KNOT AND THE OTHER ONE WAS BROKEN IN HALF.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22034844 ↗
• MalfunctionMay 16, 2025Deformation Due to Compressive Stress; Deformation Due to Compressive Stress

  IT WAS REPORTED THAT ONE OF THE INTERMITTENT CATHETERS WERE IN A KNOT AND THE OTHER ONE WAS BROKEN IN HALF. PER CUSTOMER VIA PHONE ON (B)(4) 2025, IT WAS REPORTED THAT SOME OF THE CATHETERS HAD NO HOLES AT THE END, SOME WERE BROKEN, AND SOME WERE TWISTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22034843 ↗
• MalfunctionSep 23, 2020Device Damaged Prior to Receipt by User; Manufacturing, Packaging or Shipping Problem; Device Damaged Prior to Receipt by User

  IT WAS REPORTED THAT THE PACKAGES WERE MARKED WITH 6FR, BUT THE CATHETER INSIDE WAS 8FR.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 10573430 ↗
• MalfunctionMay 26, 2020Fluid/Blood Leak; Fluid/Blood Leak; Leak/Splash; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED BY THE PATIENT'S MOTHER THAT THEY NEEDED A LARGER FRENCH SIZED CATHETER SINCE IT WAS LEAKING.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 10088472 ↗
• MalfunctionApr 4, 2020Inaccurate Flow Rate; Improper Flow or Infusion; Inaccurate Flow Rate

  IT WAS REPORTED THAT URINE DID NOT ALWAYS DRAIN FROM THE PATIENT'S BLADDER WITH USE OF THE CATHETER.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 9925893 ↗
• MalfunctionJul 18, 2019Difficult to Insert; Difficult to Insert

  IT WAS REPORTED DIFFICULT TO INSERT THE CATHETER AS IT WAS LARGER THAN USUAL. THE PATIENT WAS NOT ABLE TO FULLY INSERT THE CATHETER FOR USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8804617 ↗
• MalfunctionMay 8, 2019Incorrect Measurement; Device Markings/Labelling Problem; Incorrect Measurement

  IT WAS REPORTED THAT THE MAGIC 3 GO PEDIATRIC CATHETERS WERE LABELED 6 FRENCH, HOWEVER THE PATIENT ADVISED MANY WERE LARGER THAN THAT.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 8593638 ↗
• MalfunctionApr 4, 2019Incorrect Measurement; Inadequacy of Device Shape and/or Size; Incorrect Measurement

  IT WAS REPORTED THAT THE PEDIATRIC MAGIC 3 CATHETER WAS BIGGER THAN USUAL.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 8484329 ↗