Curos™ Tego® CTG1-270Recalls & reported problems
3m Company · 3M™ Curos™ Disinfecting Cap for Tego® Hemodialysis Connectors US - CTG1- 270 · Class U
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387773817), received between Sep 30, 2022 and Sep 30, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).
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
Device problems
- Device-Device Incompatibility1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2022Device-Device Incompatibility; Device-Device Incompatibility
A HOSPITAL ALLEGED 3M¿ CUROS¿ DISINFECTING CAP FOR TEGO® HEMODIALYSIS CONNECTOR, CTG1-270R CONNECTED TO A MALE PATIENT'S CVC [CENTRAL VENOUS CATHETER]. UPON REMOVING THE CAP, THE SPONGE WAS IN THE LUMEN OF THE CVC LINE. THE PATIENT'S CVC LINE WAS REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15520560 ↗
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- SITE-SCRUB 3882025Bard Access Systems, Inc. · Pad, alcohol, device disinfectant2 reports
- Webcol 6818Cardinal Health, Inc. · Pad, alcohol, device disinfectant2 reports
- Curos Jet™ CFJ5-2503m Company · Pad, alcohol, device disinfectant1 report
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
- 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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