Medical Action Industries 75911DRecalls & reported problems
Medical Action Industries Inc. · 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 10809160281871), received between Jul 11, 2025 and Jul 11, 2025 — classified as 1 injury.
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 Available1
Patient problems
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 11, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PATIENT HAD A REACTION (DESCRIBED AS A BURN) FOLLOWING USE OF MEDICHOICE SKIN PREP COMPONENT INCLUDED IN MEDICAL ACTION INDUSTRIES CLEAR SEQUENCE CENTRAL LINE DRESSING CHANGE KIT. THE SITE MONITORED SKIN FOR ANY INFECTION SIGNS DURING HEALING, NO FURTHER TREATMENT OR DETAILS WERE PROVIDED BY THE COMPLAINT REPORTER.
Patient problems: Burn(s)
MAUDE report 22478995 ↗
Other Central venous catheter dressing change kit devices
- Medical Action Industries 59816BMedical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- Medical Action Industries 79544BMedical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- MEDICAL ACTION INDUSTRIES 79420Medical Action Industries Inc. · Central venous catheter dressing change kit1 recall0 reports
- Medical Action Industries 74564Medical Action Industries Inc. · Central venous catheter dressing change kit3 reports
- MEDICAL ACTION INDUSTRIES 77433Medical Action Industries Inc. · Central venous catheter dressing change kit2 reports
- Medical Action Industries 58193Medical Action Industries Inc. · Central venous catheter dressing change kit1 report
- medical action industries 77993DMedical Action Industries Inc. · Central venous catheter dressing change kit1 report
- McKesson 25-2835Mckesson Medical-Surgical Inc. · Central Venous Catheter Dressing Change Kit1 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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