Medline Industries, Inc. DYNJ23764IRecalls & reported problems
Medline Industries, Inc. · HAND PACK · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10195327449728), received between Aug 27, 2025 and Aug 28, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Frayed” (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.
Reports received per month
Most reported problems
Device problems
- Material Frayed1
- Material Integrity Problem1
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2025Material Frayed; Material Frayed
ACCORDING TO THE CUSTOMER, ON (B)(6) 2025 THE SPONGE HAD A "LOOSER WEAVE THAN NORMAL" CAUSING "FUZZY PIECES" TO REMAIN WITHIN THE PATIENT'S BODY CAVITY.
Patient problems: Foreign Body In Patient
MAUDE report 22912920 ↗InjuryAug 27, 2025Material Integrity Problem; Material Integrity Problem
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- Medline Industries, Inc. DYNJ906893DMedline Industries, Inc. · Orthopedic tray4 recalls2 reports
- Medline Industries, Inc. DYNJ909505AMedline Industries, Inc. · Orthopedic tray4 recalls1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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