JACKSON-PRATT JP-2190Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380182457), received between Dec 3, 2025 and Dec 3, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Material Separation” (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-0971-2023 · 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.

• InjuryDec 3, 2025Material Separation; Material Separation

  WE HAD AN UNFORTUNATE SITUATION WITH THE CARDINAL HEALTH JACKSON-PRATT CHANNEL DRAINS JP-2190 THAT WE RECENTLY ORDERED. THE CHANNEL PART THAT GOES UNDER THE SKIN, SEPARATED FROM THE PART THAT IS OUTSIDE OF THE SKIN, THEREFORE CAUSING THE CHANNEL PART TO GET STUCK UNDER THE SKIN AND THE DOCTOR HAD TO OPEN THE AREA AND RETRIEVE THE CHANNEL PART OF THE DRAIN.

  Patient problems: Foreign Body In Patient

  MAUDE report 23710419 ↗