Magic3 Go Pediatric Catheter with SureGrip 52810GRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741136870), received between Mar 12, 2020 and Oct 29, 2025 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Incorrect Measurement” (1 report).

1 FDA recall record name this device's identifier, 1 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, 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.

Recalls naming this device

1. Apr 20, 2023Class IIOpen, Classified

   Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.

   Z-1700-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 29, 2025Incorrect Measurement; Incorrect Measurement

  IT WAS REPORTED THAT THE PATIENT SAID THE CATHETERS THEY RECEIVED WERE TOO LONG. NO MEDICAL INTERVENTION OR PATIENT IMPACT WAS REPORTED. NO ADDITIONAL INFORMATION PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23415245 ↗
• InjuryJun 6, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE INTERMITTENT CATHETER POSSIBLY CAUSED URINARY TRACT INFECTION. IT TOOK PLACE A MONTH AGO AND HAD RECEIVED ANTIBIOTICS ABOUT 3 TIMES TO OVERCOME URINARY TRACT INFECTION. PER FOLLOW UP VIA PHONE ON (B)(6) 2023, IT WAS REPORTED THAT THE CUSTOMER RECEIVED A VOLUNTARY EMERGENCY NOTICE FROM BD REGARDING A RECALL FOR A NONCONFORMITY WITH THE MAGIC GO 14 FR CATHETERS. THEY WERE REPORTED IN A COMPANY-WIDE NOTICE AS HAVING NONSTERILE COUDE, AND THEY HAPPENED TO BE ONE OF THOSE IMPACTED BY IT. AT THE TIME, THEY WERE SENT OUT FROM 180 MEDICAL. THIS LED TO NUMEROUS BLADDER INFECTIONS AND SEPSIS, AND THIS MADE THINGS DIFFICULT FOR THEM AS THEY COULD NOT WALK. THEY STILL HAD SAMPLES AVAILABLE AND PROVIDED THE LOT# JUGW1445.

  Patient problems: Sepsis; Unspecified Infection; Urinary Tract Infection

  MAUDE report 17071263 ↗
• MalfunctionMar 12, 2020Patient-Device Incompatibility; Therapeutic or Diagnostic Output Failure; Patient-Device Incompatibility

  IT WAS REPORTED THAT THE CUSTOMER WAS UNABLE TO USE MAGIC 3 GO CATHETERS. NO MEDICAL INTERVENTION WAS REPORTED.

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

  MAUDE report 9824450 ↗