Medline DYNJP1020SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10080196308125), received between Sep 23, 2026 and Sep 23, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Feb 13, 2025Open, Classified

   Potential breach in pouch packaging which could lead to loss of sterility.

   Z-1364-2025 · Root cause: Packaging process control · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

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

• MalfunctionSep 23, 2026Loss of or Failure to Bond

  It was reported that: "Since the client has been using the basic pack, the suture bag never stays stuck to the drape even when they apply strong pressure. The bag always falls, the adhesive does not hold sufficiently."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50867955 ↗