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
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
- GAMMEX 20685275Ansell Healthcare Product · Surgeon'S Gloves2 recalls0 reports
- PROTEXIS 2D72PT65XCardinal Health 200, LLC · Surgeon's gloves1 recall2 reports
- Medline Industries, Inc. DYNJ63673DMedline Industries, Inc. · Surgeon's gloves1 recall1 report
- GAMMEX 20685265Ansell Healthcare Product · Surgeon'S Gloves1 recall1 report
- NOVAPLUS V20685275Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- GAMMEX 20685290Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- NOVAPLUS V20685280Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- PROTEXIS 2D72PL65XCardinal Health 200, LLC · Surgeon's gloves1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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