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Medical Action Industries 83740Recalls & reported problems

Medical Action Industries Inc. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
10
Deaths reported
0
Injuries reported
10
Recalls naming it
0

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10809160412480), received between Apr 29, 2024 and Apr 29, 2024 — classified as 10 injuries.

The most frequently reported specific device problem is “Fitting Problem” (10 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 10 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports20242025202610
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Fitting Problem10

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available10

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT ONE OF TEN. THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT ONE OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19205927 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT NINE OF TEN THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT NINE OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19203266 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT EIGHT OF TEN THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT EIGHT OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19203235 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT SEVEN OF TEN THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT SEVEN OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19203190 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT SIX OF TEN THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT SIX OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19203019 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT FIVE OF TEN THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT FIVE OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19202975 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT FOUR OF TEN. THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT FOUR OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19202938 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT THREE OF TEN. THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT THREE OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19202891 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT TEN OF TEN. THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT TEN OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19202852 ↗
  • InjuryApr 29, 2024Fitting Problem; Fitting Problem

    INCIDENT TWO OF TEN. THE CUSTOMER REPORTED THAT NEEDLE IS BENDING DURING PROCEDURE AND NOTED THE HOLE ON THE NEEDLE IS LOCATED IN THE WRONG POSITION. THE CUSTOMER INDICATED THERE WERE TEN DIFFERENT PROCEDURES IMPACTED, THIS IS INCIDENT TWO OF TEN. THE PROCEDURES IMPACTED INCLUDE MEDIAL BRANCH BLOCK, INTERLAMINAL, CAUDAL, AND SI INJECTIONS. THERE WAS NO APPARENT PATIENT INJURIES OR INTERVENTIONS TAKEN; HOWEVER, THE COMPLAINT SITE IS NOT CERTAIN THE PROCEDURE IS FULLY SUCCESSFUL GIVEN THE NEEDLE HOLE PRESENTATION. THE COMPLAINT SITE HAS INDICATED THERE WERE DELAYS IN PROCEDURE AND CONCERN OF MEDICATION TRAVELING TO OTHER AREAS OF THE SPINE THAT WERE NOT TARGETED FOR PROCEDURE. THE PATIENTS WILL BE FURTHER EVALUATED AT THEIR FOLLOW-UP APPOINTMENTS WITH PROVIDER. THE COMPLAINT SITE HAS INDICATED THIS WAS NOT THE NEEDLE THAT THEY AGREED UPON DURING CREATION OF THE KIT.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 19202794 ↗

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