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Medline Industries, Inc. DYNDC2610ARecalls & reported problems

Medline Industries, Inc. · PICC LINE DRSG CHNG W/ BIOPTCH · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889942774173), received between Jul 30, 2019 and Jul 30, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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

  • Patient-Device Incompatibility1

Patient problems

  • Local Reaction1
  • Rash1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 30, 2019Patient-Device Incompatibility

    IT WAS REPORTED THAT PATIENT DEVELOPED REACTION TO CHLORAPREP (TAKEN FROM DRESSING CHANGE KIT). THE PATIENT REPORTEDLY REQUIRED TREATMENT WITH HIGH POTENCY STEROID CREAM (LIDEX).

    Patient problems: Local Reaction; Rash

    MAUDE report 8842553 ↗

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Sources and updates

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