Medical Action Industries 73969BRecalls & reported problems
Medical Action Industries Inc. · Kit: IV 100/Cs · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10809160019344), received between Jan 6, 2026 and Jan 6, 2026 — classified as 2 injuries.
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
- Appropriate Device Problem Term/Code Not Available2
Patient problems
- Abrasion2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 6, 2026Appropriate Device Problem Term/Code Not Available
THE CLINICIAN REPORTED THE CURRENT TOURNIQUET MATERIAL IS SIGNIFICANTLY ROUGHER THAN THE PREVIOUS BLUE VERSION AND HAS CAUSED SKIN DAMAGE IN PATIENTS WITH FRAGILE OR HIGHLY SENSITIVE SKIN, INCLUDING TEARING. HISTORICALLY, TOURNIQUETS WERE MADE OF A BLUE, SOFTER MATERIAL; HOWEVER, THE NEW WHITE TOURNIQUETS ARE NOTICEABLY ROUGHER AND LESS SUITABLE FOR PATIENTS WITH DELICATE SKIN. THE OTHER CONCERN WAS THAT IT WAS WHITE AND COULD EASILY BLEND INTO THE BED LINEN, WHICH IS ALSO CONCERNING SINCE IT IS LESS NOTICEABLE AND COULD MORE EASILY BE UNINTENTIONALLY LEFT ON THE PATIENT. THE REPORTER INDICATED THEY DON'T HAVE DETAILS AROUND A SPECIFIC INCIDENT.
Patient problems: Abrasion
MAUDE report 23976538 ↗InjuryJan 6, 2026Appropriate Device Problem Term/Code Not Available
THE CLINICIAN REPORTED THE CURRENT TOURNIQUET MATERIAL IS SIGNIFICANTLY ROUGHER THAN THE PREVIOUS BLUE VERSION AND HAS CAUSED SKIN DAMAGE IN PATIENTS WITH FRAGILE OR HIGHLY SENSITIVE SKIN, INCLUDING TEARING. HISTORICALLY, TOURNIQUETS WERE MADE OF A BLUE, SOFTER MATERIAL; HOWEVER, THE NEW WHITE TOURNIQUETS ARE NOTICEABLY ROUGHER AND LESS SUITABLE FOR PATIENTS WITH DELICATE SKIN. THE OTHER CONCERN WAS THAT IT WAS WHITE AND COULD EASILY BLEND INTO THE BED LINEN, WHICH IS ALSO CONCERNING SINCE IT IS LESS NOTICEABLE AND COULD MORE EASILY BE UNINTENTIONALLY LEFT ON THE PATIENT. THE REPORTER INDICATED THEY DON¿T HAVE DETAILS AROUND A SPECIFIC INCIDENT.
Patient problems: Abrasion
MAUDE report 23976536 ↗
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- MEDLINE DYNDV2465Medline Industries, Inc. · I.V. start kit2 recalls0 reports
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- Centurion IVS3900ACenturion Medical Products Corporation · I.V. start kit2 recalls0 reports
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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