PROTEXIS 2D72LS75Recalls & reported problems
Cardinal Health 200, LLC · Sterile Latex Powder Free Surgical Gloves with Hydrogel Coating · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380024054), received between Mar 22, 2019 and Mar 22, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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.
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 22, 2019Physical Resistance/Sticking
CASES WERE SELECTIVE CORONARY ANGIOGRAMS (SCA) WITH PERCUTANEOUS CORONARY INTERVENTIONS (PCI). DURING THE PCI THE STICKINESS OF THE GLOVES WOULD CAUSE THE CORONARY WIRE TO DISLODGE FROM THE LESION RESULTING IN THE PHYSICIAN NEEDING TO REWIRE THE LESION. PER CUSTOMER, NO ADVERSE EFFECTS TO PATIENTS OTHER THAN LENGTHENED PROCEDURE TIMES. NO ADDITIONAL PATIENT OR EVENT SPECIFICS PROVIDED BY CUSTOMER.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8443702 ↗
Other Surgeon's gloves devices
- GAMMEX 20685275Ansell Healthcare Product · Surgeon'S Gloves2 recalls0 reports
- PROTEXIS 2D72PT65XCardinal Health 200, LLC · Surgeon's gloves1 recall2 reports
- GAMMEX 20685265Ansell Healthcare Product · Surgeon'S Gloves1 recall1 report
- 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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