Magic3 Coude Intermittent Catheter with Sure-Grip SleeveRecalls & reported problems across all models
C. R. Bard, Inc. · 5 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,466
- Deaths reported
- 2
- Injuries reported
- 184
- Recalls
- 0
We found 5 models of Magic3 Coude Intermittent Catheter with Sure-Grip Sleeve by C. R. Bard, Inc. in the FDA's device registry (GUDID). Together they are named in 1,466 adverse event reports in the FDA's MAUDE database, received between Apr 11, 2017 and Sep 21, 2026 — classified as 2 deaths, 184 injuries, 1,280 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (298 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. 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
Reports received per month, all models
Most reported Magic3 Coude Intermittent Catheter with Sure-Grip Sleeve problems
Device problems
- Material Twisted/Bent298
- Improper Chemical Reaction196
- Difficult to Insert183
- Nonstandard Device158
- Product Quality Problem156
- Short Fill122
- Component Missing92
- Incorrect Measurement74
Patient problems
- No Clinical Signs, Symptoms or Conditions434
- No Known Impact Or Consequence To Patient423
- No Consequences Or Impact To Patient307
- Hemorrhage/Blood Loss/Bleeding154
- Patient Problem/Medical Problem154
- Urinary Tract Infection143
- Pain92
- No Patient Involvement83
Magic3 Coude Intermittent Catheter with Sure-Grip Sleeve models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50614CATHETER, UROLOGICAL883 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50616CATHETER, UROLOGICAL2 deaths443 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50612CATHETER, UROLOGICAL85 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50618CATHETER, UROLOGICAL42 reports
- Magic3™ Coude Intermittent Catheter with Sure-Grip™ Sleeve 50610CATHETER, UROLOGICAL13 reports
Recent Magic3 Coude Intermittent Catheter with Sure-Grip Sleeve adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Complete Blockage
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848821 ↗MalfunctionSep 11, 2026Difficult to Insert
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50739289 ↗MalfunctionSep 6, 2026Component Misassembled
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50636927 ↗MalfunctionAug 28, 2026Component Misassembled
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50508391 ↗MalfunctionAug 28, 2026Component Misassembled
It was reported that the customer states that the catheter did not work, openings were not punctured into the catheter, no suction, just one catheter so far in box. Patient has ordered this product previously.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50501979 ↗InjuryAug 26, 2026Adverse Event Without Identified Device or Use Problem
It was reported that Patient said he receives UTIs on a regular basis and wanted to see if we have any recommendations. Advised him we are not medical professionals but only go by what the Doctor recommend. Also advised him the Doctor wrote the RX for 4x a day instead of the 3x; he is currently ordering. Advised him to ask the Doctor, how many he need to be cathing a day. It's unclear if lot number was requested. No additional information provided.
Patient problems: Urinary Tract Infection
MAUDE report 50459574 ↗MalfunctionAug 26, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50452740 ↗MalfunctionAug 14, 2026Sharp Edges
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Insufficient Information; Pain
MAUDE report 50258104 ↗MalfunctionAug 11, 2026Material Twisted/Bent
It was reported that the Patient said 12 catheters were defective, the tip was a true 90 degree, and some were at 45-degree angle. No medical intervention or patient impact reported. No additional information provided. Per liberator clarification received on 30JUL2026, patient used 50616.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50208706 ↗MalfunctionAug 4, 2026Component Misassembled; Misassembly During Maintenance/Repair
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50132931 ↗InjuryJul 14, 2026Device Contaminated During Manufacture or Shipping
PATIENT RECEIVED 4 CATHETERS THAT HAD BLACK SPECKS ON THEM AFTER HE OPENED THEM UP. THE PATIENT RECEIVED A UTI. LOT#JUKX0341. NO ADDITIONAL INFORMATION PROVIDED. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED FOR URINARY TRACT INFECTION.
Patient problems: Urinary Tract Infection
MAUDE report 25820142 ↗InjuryJul 14, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY CUSTOMER THAT THE 4 HYDROPHILIC INTERMITTENT URINARY CATHETERS HAD BLACK SPECKS ON THEM AFTER IT HAD OPENED AND THEN THE PATIENT RECEIVED A URINARY TRACT INFECTION. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED FOR URINARY TRACT INFECTION. JUKX0341. JUKZ9524.
Patient problems: Urinary Tract Infection
MAUDE report 25815367 ↗InjuryJul 14, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY CUSTOMER THAT THE 4 HYDROPHILIC INTERMITTENT URINARY CATHETERS HAD BLACK SPECKS ON THEM AFTER IT HAD OPENED AND THEN THE PATIENT RECEIVED A URINARY TRACT INFECTION. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED FOR URINARY TRACT INFECTION. JUKX0341. JUKZ9524.
Patient problems: Urinary Tract Infection
MAUDE report 25815365 ↗InjuryJul 14, 2026Device Contaminated During Manufacture or Shipping
IT WAS REPORTED THAT THE PATIENT RECEIVED 4 CATHETERS THAT HAD BLACK SPECKS ON THEM AFTER HE OPENED THEM UP. THE PATIENT RECEIVED A UTI. LOT#JUKZ9524. NO ADDITIONAL INFORMATION PROVIDED. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED FOR URINARY TRACT INFECTION.
Patient problems: Urinary Tract Infection
MAUDE report 25811542 ↗MalfunctionMay 1, 2026Component Misassembled
IT WAS REPORTED THAT THE PATIENT RECEIVED ONE BOX WITH AT LEAST TWO CATHETERS NO LUBRICATION OR DRAINAGE HOLE. NO ADDITIONAL INFORMATION PROVIDED. NO TROUBLESHOOTING WAS PROVIDED. (PREPPING AND PLACEMENT TIPS SHARED).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25062270 ↗
Other C. R. Bard, Inc. products
- Bardex I.C. Foley Catheter26 models · 3,607 reports
- Bardex Lubricath Foley Catheter38 models · 1,670 reports · 1 recall
- Bardex Lubri-Sil I.C. All-Silicone Foley Catheter26 models · 1,518 reports
- Magic3 Intermittent Catheter with Sure-Grip Sleeve14 models · 1,310 reports
- Bardia Foley Catheter Silicone Coated19 models · 1,283 reports
- PureWick Female External Catheter5 models · 1,184 reports
- Bardex All-Silicone Foley Catheter12 models · 1,170 reports
- PureWick Urine Collection System3 models · 1,096 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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