Medline MSG9970Recalls & reported problems
Medline Industries, Inc. · SURG GL, SENSICARE PI ORTHO LT,LF,PF,7.0 · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10193489029857), received between Sep 10, 2026 and Sep 30, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (5 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 Torn5
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Split, Cut or Torn
It was reported that "they have had these gloves tearing at the thumb and cuff during a procedure."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950816 ↗MalfunctionSep 30, 2026Material Split, Cut or Torn
It was reported that "they have had these gloves tearing at the thumb and cuff during a procedure."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947924 ↗MalfunctionSep 29, 2026Material Split, Cut or Torn
It was reported that "One pair of gloves (with the new exp date and same box/lot) rip at the finger tips."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933237 ↗MalfunctionSep 28, 2026Material Split, Cut or Torn
It was reported that "MSG9970 GLOVES ARE RIPPING WHEN DONNING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50913898 ↗MalfunctionSep 10, 2026Material Split, Cut or Torn
It was reported that "Over the past few months, we have noticed that they are tearing when being put on But in strange locations ¿ like as if the gloves had a seam".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50719126 ↗
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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