PROTEXIS 2D72PT80XRecalls & reported problems
Cardinal Health 200, LLC · Sterile Polyisoprene Powder-Free Surgical Gloves · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380031960), received between Jul 2, 2026 and Jul 2, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Material Separation” (1 report).
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Separation1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 2, 2026Material Separation
A CUSTOMER REPORTED THAT THERE HAD BEEN AN ISSUE IN THE THEATRE ON (B)(6) 2026. THE SURGEON HAD JUST CUT INTO THE PATIENT TO INSERT SCOPE (LAPARSCOPICALLY). THE SURGEON HAD USED A CARDINAL GLOVE, AND THE GLOVE WAS REPORTED TO FEEL STICKY WHEN WET. THE SURGEON HAD BEEN HANDLING THE SCOPE, AND THE GLOVE HAD STUCK TO THE SCOPE. THE SURGEON HAD MOVED HIS HAND, AND THE GLOVE RIPPED RESULTING IN A SMALL PIECE OF GLOVE FALLING INTO PATIENT¿S ABDOMEN. IT HAD NOT BEEN RECOVERED DESPITE EXTENSIVE SEARCHING. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Foreign Body In Patient
MAUDE report 25698484 ↗
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- Medline Industries, Inc. DYNJ63673DMedline Industries, Inc. · Surgeon's gloves1 recall1 report
- GAMMEX 20685255Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- NOVAPLUS V20685265Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- NOVAPLUS V20685290Ansell Healthcare Product · Surgeon'S Gloves1 recall0 reports
- GAMMEX 20685260Ansell Healthcare Product · 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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