JACKSON-PRATT JP-2215Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380182525), received between Oct 18, 2022 and Oct 18, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

1. Dec 14, 2022Open, Classified

   Cardinal Health recently received multiple complaints regarding various performance issues with Cardinal Health Jackson-Pratt Channel Drains including lack of radiopacity in wound drains, dull trocars impacting product performance, lack of flexibility of wound drains, and broken wound tips.

   Z-0978-2023 · Root cause: Unknown/Undetermined by firm · 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.

• InjuryOct 18, 2022Difficult to Remove; Difficult to Remove

  (B)(4): PATIENT HAD JP DRAIN IN HER ABDOMEN THAT WAS ORDERED TO BE REMOVED. DURING REMOVAL OF JP DRAIN, THE TIP BROKE OFF AND MIGRATED THROUGH BODY AND HAD TO BE REMOVED THROUGH IR PROCEDURE. NO ADDITIONAL INFORMATION PROVIDED.

  Patient problems: Failure of Implant

  MAUDE report 15629615 ↗