Medline Industries, Inc. DYNJ65602ARecalls & reported problems
Medline Industries, Inc. · TOTAL KNEE PACK · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10195327048662), received between Jun 13, 2024 and Sep 10, 2024 — classified as 5 injuries.
The most frequently reported specific device problem is “Material Frayed” (3 reports).
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 Frayed3
- Degraded1
- Unraveled Material1
Patient problems
- Foreign Body In Patient5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2024Material Frayed; Material Frayed
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE LAP SPONGES IN THE PACK WERE "FRAYING" WHEN USING THEM INSIDE THE WOUND.
Patient problems: Foreign Body In Patient
MAUDE report 20181048 ↗InjurySep 5, 2024Material Frayed; Material Frayed
ACCORDING TO THE CUSTOMER, THERE HAVE BEEN MULTIPLE INCIDENTS OF THE LAP SPONGES "FRAYING" WHEN THEY ARE "UNFOLDING/ APPLY THE LAP SPONGES TO OPEN BONE".
Patient problems: Foreign Body In Patient
MAUDE report 20146749 ↗InjuryJun 14, 2024Degraded; Degraded
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE "LAP SPONGES LINTED OFF" DURING A "TOTAL KNEE" PROCEDURE. THE CUSTOMER REPORTED IT "LOOKED LIKE SNOW".
Patient problems: Foreign Body In Patient
MAUDE report 19536849 ↗InjuryJun 14, 2024Material Frayed; Material Frayed
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 "LINT" WAS NOTED ON THE "STERILE LAPS/SPONGES", "ON SURGICAL SITE", AND "FLOATING IN AIR WITH USE" DURING A PROCEDURE.
Patient problems: Foreign Body In Patient
MAUDE report 19536722 ↗InjuryJun 13, 2024Unraveled Material; Unraveled Material
ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE "LAPS" WERE "UNRAVELING" AND LEAVING "STRINGS" INSIDE THE PATIENT DURING A PROCEDURE.
Patient problems: Foreign Body In Patient
MAUDE report 19530442 ↗
Other Orthopedic tray devices
- Medline Industries, Inc. DYNJ900718CMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ905330BMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ17452SMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ21826RMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. CDS780119VMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- Medline Industries, Inc. DYNJ902473LMedline Industries, Inc. · Orthopedic tray5 recalls0 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page