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Curity 6822Recalls & reported problems

Cardinal Health, Inc. · X-Ray Detectable Laparotomy Sponges · 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 10884521128934), received between Oct 23, 2017 and Oct 23, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Incomplete or Missing Packaging” (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

  • Incomplete or Missing Packaging1

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.

  • MalfunctionOct 23, 2017Incomplete or Missing Packaging; Incomplete or Missing Packaging

    THE CUSTOMER REPORTS THAT THERE WAS ONLY 4 EACH OF SPONGES IN THE PACKAGING BAND WHICH SHOULD CONTAIN 5 EACH.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6970028 ↗

Other GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE devices

All GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.