PremierPro 5042Recalls & reported problems
Prestige Ameritech, Ltd. · PremierPro PF Plus Nitrile Exam Glove Small 200count · Class 1
- 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 00818566011985), received between Nov 14, 2024 and Nov 14, 2024 — classified as 1 malfunction.
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
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 14, 2024
REGISTERED NURSE (RN) WENT TO GRAB CHEMO GLOVES OUT OF BOX AND GLOVE RIPPED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20683030 ↗
Other Patient Examination Glove, Specialty devices
- PremierPro D5061Prestige Ameritech, Ltd. · Patient Examination Glove, Specialty1 recall0 reports
- PremierPro D5064Prestige Ameritech, Ltd. · Patient Examination Glove, Specialty1 recall0 reports
- PremierPro D5062Prestige Ameritech, Ltd. · Patient Examination Glove, Specialty1 recall0 reports
- PremierPro D5065Prestige Ameritech, Ltd. · Patient Examination Glove, Specialty1 recall0 reports
- PremierPro D5063Prestige Ameritech, Ltd. · Patient Examination Glove, Specialty1 recall0 reports
- Halyard 55090O&M Halyard, Inc. · Patient examination glove, specialty2 reports
- Halyard 47375O&M Halyard, Inc. · Patient examination glove, specialty2 reports
- FLEXAL 88FS03MCardinal Health 200, LLC · Patient examination glove, specialty1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.