Medical Action Industries 71375Recalls & reported problems
Medical Action Industries Inc. · Inst:Clamp Gomco 1.3 w/Instruc 20/Cs · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10809160023631), received between May 7, 2024 and May 10, 2024 — classified as 7 injuries.
The most frequently reported specific device problem is “Fitting Problem” (7 reports).
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
- Fitting Problem7
Patient problems
- Hemorrhage/Blood Loss/Bleeding7
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjuryMay 10, 2024Fitting Problem; Fitting Problem
CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON APRIL 11, 2024 THE CUSTOMER REPORTED BY MEDWATCH REPORT 100117-2024-0004 THAT THERE WAS A SMALL AMOUNT OF BLEEDING AFTER CIRCUMCISION PROCEDURE. SILVER NITRATE WAS APPLIED; HOWEVER, OOZING CONTINUED. SURGICEL WAS APPLIED AND GOOD HEMOSTASIS WAS ACHIEVED.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19287039 ↗InjuryMay 10, 2024Fitting Problem; Fitting Problem
INCIDENT FOUR OF SEVEN THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON APRIL 11, 2024, IT WAS REPORTED BY MEDWATCH REPORT 1000880000-2024-0004 THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. PRESSURE AND SILVER NITRATE WAS APPLIED TO BLEEDING AREA TO ACHIEVE HEMOSTASIS. ESTIMATED BLOOD LOSS WAS MINIMAL.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19287012 ↗InjuryMay 8, 2024Fitting Problem; Fitting Problem
INCIDENT ONE OF SEVEN. THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON APRIL 11, 2024 THE CUSTOMER REPORTED BY MEDWATCH REPORT (B)(4) THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. PRESSURE WAS APPLIED WITHOUT RELIEF, THE SITE CAREFULLY APPLIED SILVER NITRATE TO THE AREA OF ACTIVE BLEEDING TO ACHIEVE HEMOSTASIS. ESTIMATED BLOOD LOSS WAS <10ML.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19274828 ↗InjuryMay 7, 2024Fitting Problem; Fitting Problem
INCIDENT FIVE OF SEVEN. THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON (B)(6), 2024 THE CUSTOMER REPORTED BY MEDWATCH (B)(4) THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. PRESSURE AND SILVER NITRATE WAS APPLIED TO THE AREA OF ACTIVE BLEEDING. A SINGLE FIGURE OF 8 4-0 VICRYL SUTURE WAS APPLIED TO EDGES OF FORESKIN FOR HEMOSTASIS.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19265763 ↗InjuryMay 7, 2024Fitting Problem; Fitting Problem
INCIDENT SEVEN OF SEVEN. THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON (B)(6) 2024 THE CUSTOMER REPORTED THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. PRESSURE WAS APPLIED WITHOUT RELIEF, THE SITE CAREFULLY APPLIED SILVER NITRATE TO THE AREA OF ACTIVE BLEEDING TO ACHIEVE HEMOSTASIS. MEDWATCH REPORTS WERE RECEIVED FOR THE OTHER SIX INCIDENTS; HOWEVER, A MEDWATCH REPORT WAS NOT RECEIVED FOR THIS INCIDENT REPORTED BY CUSTOMER.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19265759 ↗InjuryMay 7, 2024Fitting Problem; Fitting Problem
INCIDENT THREE OF SEVEN. THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. ON APR 11, 2024, IT WAS REPORTED BY MEDWATCH REPORT (B)(4) THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. THE SITE WAS ABLE TO ACHIEVE HEMOSTASIS AFTER SEVERAL MINUTES WITH CONTINUOUS PRESSURE AND SILVER NITRATE. ESTIMATED BLOOD LOSS WAS MINIMAL.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19265061 ↗InjuryMay 7, 2024Fitting Problem; Fitting Problem
INCIDENT TWO OF SEVEN THE NURSE REPORTED THAT THE CLAMPS ARE SLIPPING AND CAUSING BLEEDING. IT WAS REPORTED BY MEDWATCH REPORT 100117-2024-0002 THAT BLEEDING OCCURRED AFTER THE CIRCUMCISION PROCEDURE. PRESSURE WAS APPLIED WITHOUT RELIEF, THE SITE CAREFULLY APPLIED SILVER NITRATE TO THE AREA OF ACTIVE BLEEDING TO ACHIEVE HEMOSTASIS. ESTIMATED BLOOD LOSS WAS <10ML.
Patient problems: Hemorrhage/Blood Loss/Bleeding
MAUDE report 19259178 ↗
Other CLAMP, CIRCUMCISION devices
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- Centurion CR3145KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION2 recalls0 reports
- Centurion 330CRKCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall8 reports
- Centurion 310CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall4 reports
- Centurion 330CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall1 report
- Centurion CR345KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 3145CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 345CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 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.
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