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CARDINAL HEALTH 11450-040 (UDI 20630140013758)Recalls & reported problems

Cardinal Health 200, LLC · HOT PACK NONTOXIC 1CA/4BX/10EA INSTANT 6IN X 6.5IN DISPOSABLE MEDIUM FOOD GRADE · Class 1

Data updated Oct 18, 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 20630140013758), received between Jun 13, 2019 and Jun 13, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Leak/Splash” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Leak/Splash1

Patient problems

  • Chemical Exposure1
  • Corneal Abrasion1
  • Eye Injury1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 13, 2019Leak/Splash

    BASED ON INFORMATION RECEIVED FROM THE CUSTOMER, THE HOT PACK ALLEGEDLY SPRAYED INTO A REGISTERED NURSE'S EYE REPORTEDLY CAUSING A SCRATCHED CORNEA AS THE CRYSTALS BEGAN TO FORM. THE REGISTERED NURSE WAS SEEN IN EMPLOYEE HEALTH. NO FURTHER INFORMATION WAS PROVIDED BY THE CUSTOMER DUE TO PROTECTED HEALTH INFORMATION (PHI).

    Patient problems: Chemical Exposure; Corneal Abrasion; Eye Injury

    MAUDE report 8695576 ↗

Other PACK, HOT OR COLD, DISPOSABLE devices

All PACK, HOT OR COLD, DISPOSABLE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page