Magic3 Go Intermittent Urinary Catheter 50810GRecalls & reported problems
C. R. Bard, Inc. · Magic3 Go 10 Fr Male Coudé Catheter with SureGrip · Class 2
All models of Magic3 Go Intermittent Urinary Catheter (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741137006), received between Apr 9, 2020 and Feb 21, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (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.
Reports received per month
Recalls naming this device
- 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-1699-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Deformation Due to Compressive Stress1
- Improper Chemical Reaction1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
- Patient Problem/Medical Problem1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 21, 2025Improper Chemical Reaction; Improper Chemical Reaction
IT WAS REPORTED THAT THERE WAS NOT ENOUGH LUBE ON THE INTERMITTENT CATHETERS. PATIENT ALSO SAID THE PACKAGING WAS HARD TO OPEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21432083 ↗MalfunctionApr 9, 2020Deformation Due to Compressive Stress; Material Twisted/Bent; Deformation Due to Compressive Stress
IT WAS REPORTED THAT THE PATIENT SAID HE FOLDED THE PACKAGING AND IT DID NOT GO BACK TO STRAIGHT AND IT HURT HIM. NO MEDICAL INTERVENTION REPORTED. PER FOLLOW UP RECEIVED ON 9APR2020, THE CUSTOMER STATED THAT HE PLACED THE CATHETER IN HIS POCKET AND WHEN HE TOOK IT OUT HE NOTICED THAT THE CATHETER WAS BENT. IN ADDITION THE CUSTOMER STATED HE RECEIVED 50812G CATHETERS THAT WERE DIFFERENT DIAMETERS AND UNABLE TO BE USED AND THE END WAS THIN.
Patient problems: No Known Impact Or Consequence To Patient; Patient Problem/Medical Problem
MAUDE report 9944476 ↗
Other CATHETER, STRAIGHT devices
- Magic3 Go Male Catheter with SureGrip 53814GC. R. Bard, Inc. · CATHETER, STRAIGHT1 recall490 reports
- Magic3 Go Male Coude Catheter with SureGrip 50814GC. R. Bard, Inc. · CATHETER, STRAIGHT1 recall3 deaths416 reports
- Magic3 Go™ Intermittent Urinary Catheter 51814C. R. Bard, Inc. · CATHETER, STRAIGHT1 recall327 reports
- Magic3 Go Male Coude Catheter with SureGrip 50816GC. R. Bard, Inc. · CATHETER, STRAIGHT1 recall239 reports
- Magic3 Go Male Catheter with SureGrip 53816GC. R. Bard, Inc. · CATHETER, STRAIGHT1 recall164 reports
- Magic3 Go Male Catheter with SureGrip 53812GC. R. Bard, Inc. · CATHETER, STRAIGHT1 recall120 reports
- Magic3 Go™ Intermittent Urinary Catheter 51812C. R. Bard, Inc. · CATHETER, STRAIGHT1 recall109 reports
- CURE CATHETER HM14Convatec, Purchasing Department · Catheter, Straight154 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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