Webcol 6818 (UDI 20884527020642)Recalls & reported problems
Cardinal Health, Inc. · Alcohol Prep,2 Ply, Medium · Class U
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884527020642), received between Apr 4, 2019 and May 8, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping 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 16, 2026.
Most reported problems
Device problems
- Manufacturing, Packaging or Shipping Problem1
- Moisture or Humidity Problem1
- Product Quality Problem1
Patient problems
- No Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 8, 2019Product Quality Problem
MULTIPLE COMPLAINTS HAVE BEEN RECEIVED REGARDING ALCOHOL PREP PADS BEING DRY UPON OPENING. THE FOLLOWING ARE THE DATES, UNITS, AND MAGNITUDE OF THE COMPLAINTS. A PROGRESSIVE CARE NURSE NOTED USING 3 PREP PADS ON A SINGLE PATIENT BEFORE THE FOURTH PAD HAVE ENOUGH MOISTURE TO COMPLETE THE JOB. LOT NUMBERS WERE NOT NOTED. AN ORTHOPEDIC NURSE NOTED DRYNESS IN ALCOHOL PREP PADS OVER THE COURSE OF 2-3 WEEKS. LOT NUMBERS, AGAIN, WERE NOT RECORDED. PRE-OP/PACU NURSE NOTED DRYNESS IN ALCOHOL PREP PADS OVER THE COURSE OF MULTIPLE WEEKS. MANUFACTURER RESPONSE FOR PAD, ALCOHOL, DEVICE DISINFECTANT, WEBCOL (PER SITE REPORTER). THE MANUFACTURER WAS NOTIFIED VIA PURCHASING DEPARTMENT. RESPONSE IS UNCERTAIN. MANUFACTURER RESPONSE FOR PAD, ALCOHOL, DEVICE DISINFECTANT, WEBCOL (PER SITE REPORTER). THE MANUFACTURER WAS NOTIFIED VIA PURCHASING DEPARTMENT. RESPONSE IS UNCERTAIN. MANUFACTURER RESPONSE FOR PAD, ALCOHOL, DEVICE DISINFECTANT, WEBCOL (PER SITE REPORTER). THE MANUFACTURER WAS NOTIFIED VIA PURCHASING DEPARTMENT. RESPONSE IS UNCERTAIN.
Patient problems: No Information
MAUDE report 8593691 ↗MalfunctionApr 4, 2019Manufacturing, Packaging or Shipping Problem; Moisture or Humidity Problem
RN OPENED APPROXIMATELY 18 COVIDIEN WEBCOL ALCOHOL PREPS WHERE THE PAD WAS DRY. ADDITIONALLY, THE PADS TO NOT SMELL AS IF THEY EVER CONTAINED ANY ISOPROPYL ALCOHOL.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8482000 ↗
Other Pad, alcohol, device disinfectant devices
- MEDLINE DYNDA2723Centurion Medical Products Corporation · Pad, alcohol, device disinfectant1 recall0 reports
- Webcol 5110Cardinal Health 200, LLC · Pad, alcohol, device disinfectant16 reports
- BD PosiFlush SureScrub 306559Becton, Dickinson And Company · Pad, alcohol, device disinfectant15 reports
- 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 200, LLC · Pad, alcohol, device disinfectant1 report
- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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