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CARDINAL HEALTH POV2THA110Recalls & reported problems

Cardinal Health 200, LLC · KIT, TOTAL HIP, PRESBYTERIAN · 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 10195594777975), received between Oct 14, 2022 and Oct 14, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

  • Break1

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.

  • InjuryOct 14, 2022Break; Break

    CUSTOMER REPORTED SUCTION TIP BROKE INSIDE PATIENT FEMUR BONE DURING TOTAL HIP CASE. THE ITEM IS RETAINED IN PATIENT, BUT NO FURTHER INJURY REPORTED. ¿DISCLOSURE MADE TO THE PATIENT REGARDING DECISION NOT TO DO ANYTHING FURTHER TO REMOVE IT SINCE THE RISKS OUTWEIGHED BENEFITS."

    Patient problems: Foreign Body In Patient

    MAUDE report 15611169 ↗

Other Orthopedic tray devices

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Sources and updates

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