Medical Action Industries 75431Recalls & reported problems
Medical Action Industries Inc. · Kit: Suture Removal 50/Cs PILOT · Class 1
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 10809160022436), received between Oct 7, 2024 and Oct 7, 2024 — classified as 1 malfunction.
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
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 7, 2024
WHILE USING THE DISPOSABLE HEMOSTAT, THE TIP BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20384900 ↗
Other Suture removal kit devices
- MEDLINE 86125Medline Industries, Inc. · Suture removal kit1 recall0 reports
- Medline Industries, Inc. DYNDR1277AMedline Industries, Inc. · Suture removal kit1 recall0 reports
- MEDLINE TRI44105Medline Industries, Inc. · Suture removal kit1 recall0 reports
- MEDLINE 60280Medline Industries, Inc. · Suture removal kit1 recall0 reports
- Centurion 60265Centurion Medical Products Corporation · Suture removal kit1 recall0 reports
- Medline Industries, Inc. DYNDA2936Medline Industries, Inc. · Suture removal kit1 recall0 reports
- MEDLINE TRI55405Medline Industries, Inc. · Suture removal kit1 recall0 reports
- MEDLINE SR60555Medline Industries, Inc. · Suture removal kit1 recall0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page