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CARDINAL HEALTH PG40LCKGKRecalls & reported problems

Cardinal Health 200, LLC · KIT, LAP CHOLE · Class 2

Data updated Oct 18, 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 10887488975948), received between Nov 19, 2018 and Nov 19, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Component Missing” (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

  • Component Missing1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionNov 19, 2018Component Missing

    CARDINAL HEALTH CUSTOM PACK #PG40LCKGK LOT#500785 MISSING ONE TAG SPONGE. SHOULD BE PACK OF 5. SPONGES REMOVED FROM ROOM PER POLICY.

    Patient problems: No Information

    MAUDE report 8084074 ↗

Other laparoscopy kit devices

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Sources and updates

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