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MEDLINE MSG9060Recalls & reported problems

Medline Industries, Inc. · GLOVE,SURG,SENSICARE PI,LF,PF,6.0 · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
15
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 10888277347878), received between Mar 31, 2026 and Sep 25, 2026 — classified as 15 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (13 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 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 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: 1 reportsApr 2026: 0 reportsMay 2026: 2 reportsJun 2026: 5 reportsJul 2026: 2 reportsAug 2026: 1 reportsSep 2026: 4 reportsOct 2026: 0 reports2024202520265
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Material Split, Cut or Torn13
  • Material Integrity Problem2
  • Inadequacy of Device Shape and/or Size1

Patient problems

  • No Clinical Signs, Symptoms or Conditions14
  • Numbness1

Recent adverse event reports

The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 25, 2026Material Split, Cut or Torn

    It was reported that Sterile gloves are tearing when being put on.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50899781 ↗
  • MalfunctionSep 8, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50676221 ↗
  • MalfunctionSep 2, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50568438 ↗
  • MalfunctionSep 2, 2026Inadequacy of Device Shape and/or Size; Material Split, Cut or Torn

    Patient problems: Numbness

    MAUDE report 50564182 ↗
  • MalfunctionAug 31, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50532184 ↗
  • MalfunctionJul 9, 2026Material Split, Cut or Torn

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25771338 ↗
  • MalfunctionJul 2, 2026Material Split, Cut or Torn

    IT WAS REPORTED BY THE CUSTOMER THAT THE GLOVES ARE RIPPING WHILE DONNING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25689117 ↗
  • MalfunctionJun 22, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT THE GLOVES ARE TEARING WHEN THEY ARE PUT ON.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25586213 ↗
  • MalfunctionJun 19, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT "THE SURGEON WAS GLOVING HERSELF AND THE GLOVE TORE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25566144 ↗
  • MalfunctionJun 19, 2026Material Integrity Problem

    IT WAS REPORTED THAT "THE SURGEON WAS GLOVING HERSELF AND THE GLOVE TORE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25566139 ↗
  • MalfunctionJun 18, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT THE DEVICE WAS "TORN UPON PUTTING ON" AND OCCURRED WHILE "PUTTING GLOVES ON SURGEON PRIOR TO THE START OF A STERILE SURGICAL PROCEDURE...NO EFFECT - DID NOT REACH PATIENT/PERSON - DETECTED BEFORE USE OR DOES NOT TOUCH PATIENT DURING USE". IT WAS ALSO REPORTED THAT THIS OCCURRED DURING A "LAPAROSCOPIC CASE" AND HAS HAPPENED "MULTIPLE TIMES".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25551642 ↗
  • MalfunctionJun 16, 2026Material Integrity Problem

    ACCORDING TO THE FACILITY ON (B)(6), THE GLOVES TORE UPON PUTTING THEM ON A SURGEON FOR A STERILE SURGICAL PROCEDURE (A LAPAROSCOPIC CASE). THERE WAS NO HARM. IT WAS DETECTED PRIOR TO PATIENT USE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25523383 ↗
  • MalfunctionMay 27, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT THE GLOVES TEAR EASILY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25302580 ↗
  • MalfunctionMay 23, 2026Material Split, Cut or Torn

    IT WAS REPORTED THAT, WHEN GLOVING SURGEON, GLOVES RIPPED. DID NOT REACH PATIENT/PERSON.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25266323 ↗
  • MalfunctionMar 31, 2026Material Split, Cut or Torn

    AS PER ACCOUNT, DURING SURGERY - SURGEON REQUIRED NEW GLOVES - TORN AS SCRUB NURSE WAS PUTTING GLOVES ON SURGEON. PACK HAS A BIT OF BLOOD DRIED ON IT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24746872 ↗

Other Surgeon's gloves devices

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Sources and updates

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