FDA Adverse Event
Malfunction
Summary report: N
VARISOFT INFUSION SET
MDR report key: 24119531
·
Received January 20, 2026
Report
- Report Number
- MW5182507
- Event Type
- Malfunction
- Date Received
- January 20, 2026
- Date of Event
- January 11, 2026
- Report Date
- January 13, 2026
- Manufacturer
- UNOMEDICAL A/S
- Product Code
- FPA
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- NY, US
- Reporter Occupation
- PATIENT
- Health Professional
- *
Narratives
Description of Event or Problem · 0
I USE VARISOFT INFUSION SETS. THE TUBING WORE AWAY/RIPPED OFF AT THE CONNECTION TO MY T-SLIM INSULIN PUMP. THE TUBING LOOKED LIKE IT WAS WORN AWAY AS IT LOOKED VERY THIN, KINDA LIKE IF YOU PULL AND BEND A PLASTIC TUBE IT WILL EVENTUALLY BREAK. THIS IS THE THIRD TIME THIS HAS HAPPENED IN THE LAST MONTH. THE FIRST TWO TIMES IT HAPPENED; I BLAMED IT ON A NEW PUMP CASE I WAS USING. HOWEVER, THE THIRD TIME IT HAPPED, I HAD SWITCHED BACK TO MY OLD CASE WHICH I HAD BEEN USING FOR THE PAST 4+ YEARS AND NEVER HAD THIS PROBLEM. UNFORTUNATELY, I DIDN'T GET PHOTOS OF THE SET, AS IT DIDN'T OCCUR TO ME THAT IT COULD BE A FAULTY INFUSION SET UNTIL I GOOGLED IT. PATIENT CODE: 1905. DEVICE CODE: 1153; 4008. REFERENCE REPORT#: MW5182508; MW5182509.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 174226 | VARISOFT INFUSION SET | SET, ADMINISTRATION, INTRAVASCULAR | FPA | UNOMEDICAL A/S | 1002828 | 6012517 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 54 YR | Female | Other | ALENDRONATE SODIUM.| ALEVE.| ATORVASTATIN.| CALCIUM.| DEXCOM G6 CONTINUOUS GLUCOSE MONITOR.| DILTIAZEM.| HUMALOG INSULIN.| MAGNESIUM.| TANDEM T-SLIM INSULIN PUMP.| TYLENOL.| VITAMIN D.| ZINC. |