MEDLINE DYNDC3285Recalls & reported problems
Medline Industries, Inc. · DBL DRAPE CENTRAL LINE KIT · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10653160358190), received between Sep 9, 2024 and Sep 10, 2024 — classified as 6 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (4 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem4
- Appropriate Device Problem Term/Code Not Available2
Patient problems
- Skin Inflammation/ Irritation4
- Skin Disorders2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2024 SKIN ISSUES WERE REPORTED WITH THE CHG GEL DRESSING DESCRIBED AS "WOUND WITH PRESENCE OF SLOUGH AT TIMES".
Patient problems: Skin Disorders
MAUDE report 20181531 ↗InjurySep 10, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ACCORDING TO THE FACILITY ON 08/02/2024 SKIN ISSUES WERE REPORTED WITH THE CHG GEL DRESSING DESCRIBED AS "WOUND WITH PRESENCE OF SLOUGH AT TIMES".
Patient problems: Skin Inflammation/ Irritation
MAUDE report 20181382 ↗InjurySep 10, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ACCORDING TO THE FACILITY ON (B)(6) 2024 SKIN ISSUES WERE REPORTED WITH THE CHG GEL DRESSING DESCRIBED AS "WOUND WITH PRESENCE OF SLOUGH AT TIMES".
Patient problems: Skin Inflammation/ Irritation
MAUDE report 20181031 ↗InjurySep 9, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2024 SKIN ISSUES WERE REPORTED WITH THE CHG GEL DRESSING DESCRIBED AS "WOUND WITH PRESENCE OF SLOUGH AT TIMES".
Patient problems: Skin Disorders
MAUDE report 20176982 ↗InjurySep 9, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjurySep 9, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
Other TRAY, SURGICAL devices
- MEDLINE DYNDA2526Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1534Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1470BMedline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- Centurion MNS11625Centurion Medical Products Corporation · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYKM1756AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE SPEC0291BMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYNDC3188Medline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYNDH1542Medline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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