Medline MSG9980Recalls & reported problems
Medline Industries, Inc. · SURG GL,SENSICARE PI ORTHO LT,LF,PF,8.0 · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10193489029871), received between May 11, 2026 and Sep 30, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (6 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 Torn6
- Physical Resistance/Sticking2
- Material Puncture/Hole1
- Structural Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
- Exposure to Body Fluids1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Puncture/Hole
It was reported that "hole punch out of glove; saw this is 3 different pairs."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50949353 ↗MalfunctionSep 29, 2026Material Split, Cut or Torn
It was reported that "torn when putting on."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50932249 ↗MalfunctionSep 28, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916075 ↗MalfunctionSep 9, 2026Material Split, Cut or Torn
Patient problems: Exposure to Body Fluids
MAUDE report 50698072 ↗MalfunctionSep 2, 2026Physical Resistance/Sticking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50564793 ↗MalfunctionSep 1, 2026Material Split, Cut or Torn
It was reported that "It seems their Sensicare PI Ortho LT gloves have been ripping easily, and they claimed to go through 26 pairs of gloves in one case."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50551555 ↗MalfunctionAug 31, 2026Structural Problem; Physical Resistance/Sticking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50532346 ↗MalfunctionMay 22, 2026Material Split, Cut or Torn
IT WAS REPORTED THAT, THE STAFF AND DOCTORS ARE COMPLAINING THAT THE GLOVES ARE TEARING DURING DONNING. AN ADDITIONAL COMPLAINT IS THE GLOVES FALLING DOWN AND TECHS END UP WITH BLOOD IN THEIR GLOVES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25251034 ↗MalfunctionMay 11, 2026Material Split, Cut or Torn
ACCORDING TO THE CUSTOMER, AS SURGICAL TECH WAS DONNING SURGEON LEFT GLOVE BROKE AT CUFF AS THEY WERE TRYING TO OPEN IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25133796 ↗
Other Surgeon's gloves devices
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- 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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