Curos™ CFF1-270Recalls & reported problems
3m Company · 3M™ Curos™ Disinfecting Cap for Needleless Connectors 270/Carton 20 Cartons/Case CFF1-270 · 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 30707387773756), received between Jun 15, 2020 and Jun 15, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 15, 2020Use of Device Problem; Use of Device Problem
EU AUTHORITIES ((B)(6)) REPORTED A HOSPITAL ALLEGED PART OF THE SPONGE FROM THE CAP OF CFF1-270R 3M¿ CUROS¿ DISINFECTING CAP FOR NEEDLELESS CONNECTOR WAS IN THE LIMB OF A HEMODIALYSIS CATHETER. THE SPONGE WAS REMOVED VIA SYRINGE. NO INJURIES WERE ALLEGED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10153939 ↗
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- SITE-SCRUB 3882100Bard Access Systems, Inc. · Pad, alcohol, device disinfectant8 reports
- Curos Jet™ CFJ1-2703m Company · Pad, alcohol, device disinfectant3 reports
- 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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