QUIKCLOT IPN926809Recalls & reported problems
Teleflex Incorporated · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841495150026), received between Jan 3, 2025 and Jan 3, 2025 — classified as 1 injury.
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.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 3, 2025Use of Device Problem; Use of Device Problem
TRAUMA PATIENT CAME IN FROM CAR ACCIDENT. QC C+ WAS USED TO PACK LIVER BLEED, PATENT WENT TO ICU AND NEXT DAY WENT TO X-RAY. RADIOLOGIST WAS NOT AWARE OF QC BEING LEFT IN THE PATIENT AND COULD NOT SEE ANY DETECTION AT FIRST PASS/INITIAL READ. PRODUCT WAS LEFT IN PATIENT AND RADIOLOGIST TOOK A SECOND LOOK AND WAS ABLE TO SEE THE X-RAY DETECTABLE STRIP THE SECOND TIME. PRODUCT WAS IN FOR AT LEAST 24 HRS. ALL PRODUCT WAS REMOVED AT THIS TIME. SOUNDS LIKE THERE IS NO PATIENT HARM. THE PATIENT RETURNED TO SURGERY AFTER IT WAS DISCOVERED THE Z-FOLD WAS LEFT IN PLACE INADVERTENTLY. THEY RETURNED TO SURGERY AND IT WAS REMOVED SUCCESSFULLY. THE CONCERN WAS THAT THE Z-FOLD IS NOT EASILY RECOGNIZABLE ON AN XRAY.
Patient problems: Insufficient Information
MAUDE report 21065101 ↗
Other Temporary, internal use hemostatic devices
- QuikClot 4030Z-Medica, LLC · Temporary, Internal Use Hemostatic1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page