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Medline Industries, Inc. DYNJ33657BRecalls & reported problems

Medline Industries, Inc. · BILLINGS CLINIC SC T&A PACK · Class 1

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 10889942576081), received between Jul 20, 2020 and Jul 20, 2020 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

  • MalfunctionJul 20, 2020Incomplete or Missing Packaging

    SC T&A PACK MADE BY MEDLINE IS SUPPOSED TO CONTAIN 10-4X4 GAUZE PADS. THE PACK CAME SEALED WITH ONLY 6-4X4 GAUZE PADS. THE PACK WAS OPENED IN THE OR FOR THE UPCOMING CASE. A COUNT OF 6-4X4 GAUZE PADS WERE FOUND INSTEAD OF THE EXPECTED 10. THE ROOM AND PATIENT WERE DOUBLE CHECKED JUST IN CASE THEY FELL WHILE OPENING THE PACK. THE COUNT OF 6 WAS CORRECT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10294792 ↗

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Sources and updates

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