Medline Industries, Inc. DYND40615Recalls & reported problems
Medline Industries, Inc. · TRAY, TRACHEOSTOMY CLEAN CARE · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10080196032884), received between Aug 14, 2024 and Aug 21, 2024 — classified as 3 injuries.
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
- Appropriate Device Problem Term/Code Not Available3
Patient problems
- Insufficient Information3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryAug 21, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, "THE BRUSHES ARE SHEDDING AND LEAVING THE BRISTLES AND OTHER DEBRIS IN HIS STOMA. THEY HAVE HAD TO CLEAN LITTLE BRISTLES OUT OF HIS STOMA SO HE DOES NOT INGEST THEM."
Patient problems: Insufficient Information
MAUDE report 20022516 ↗InjuryAug 21, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, "THE BRUSHES ARE SHEDDING AND LEAVING THE BRISTLES AND OTHER DEBRIS IN HIS STOMA. THEY HAVE HAD TO CLEAN LITTLE BRISTLES OUT OF HIS STOMA SO HE DOES NOT INGEST THEM."
Patient problems: Insufficient Information
MAUDE report 20020489 ↗InjuryAug 14, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, "THE BRUSHES ARE SHEDDING AND LEAVING THE BRISTLES AND OTHER DEBRIS IN HIS STOMA."
Patient problems: Insufficient Information
MAUDE report 19984487 ↗
Other AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY devices
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- Medline DYND300015PMedline Industries, Inc. · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- KING LTS-D Kit KLTSD430King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- Medline DYND300040PMedline Industries, Inc. · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- King LTS-D KLTSD421King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 reports
- ONE-PIECE GUEDEL AIRWAY, SIZE 3, ISO 9 1113090Intersurgical Incorporated · Airway, Oropharyngeal, Anesthesiology1 recall0 reports
- KING LTS-D Kit KLTSD432King Systems Corporation · AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY1 recall0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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