JACKSON-PRATT JP-2225Recalls & reported problems
Cardinal Health 200, LLC · JP CHAN DRN SIL RND 19FR 3/4 W/TRO · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885380182570), received between Apr 5, 2024 and May 26, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 reports).
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.
Reports received per month
Recalls naming this device
- 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-0983-2023 · Root cause: Unknown/Undetermined by firm · FDA record ↗
Most reported problems
Device problems
- Break2
Patient problems
- Foreign Body In Patient1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 26, 2024Break; Break
MW5153800: CUSTOMER REPORTED THAT JACKSON-PRATT DRAIN WAS PLACED IN PATIENT MONDAY, FOLLOWING PANNICULECTOMY. PATIENT EVALUATED WITH JP TUBING AMPUTATED AT GLUED PORTION OF TUBING AND TUNNELING DEVICE CONSISTENT WITH FAILED/FAULTY JP DRAIN. TUNNELED TUBING WAS EMBEDDED INTO THE ABDOMINAL WALL REQUIRING REPEAT SURGERY AND REMOVAL OF FOREIGN BODY. NO OTHER MANUFACTURER JP DRAIN AVAILABLE. PATIENT WAS DISCHARGED WITHOUT SEQUELA.
Patient problems: Foreign Body In Patient
MAUDE report 19399229 ↗InjuryApr 5, 2024Break; Break
CUSTOMER REPORTED THAT THE PRODUCT WAS PLACED EARLY LAST WEEK. PATIENT WENT TO ANOTHER UNIT AND THE DRAIN WASN¿T PRODUCING ANYTHING. THE DOCTOR ASSUMED IT WAS JUST THE BULB THAT WAS THE ISSUE, SO SHE REPLACED THE BULB. NOTHING RESULTED FROM THIS. IT TURNED OUT THERE WAS AN AIR LEAK WHICH CAUSED THE DRAIN TO HAVE NO SUCTION. WHEN THE DOCTOR WENT TO MANIPULATE THE ACTUAL DRAIN LINE IT FELL APART AND COMPLETELY PULLED OUT WITH THE SUTURE ATTACHED TO THE END. NO FURTHER INFORMATION PROVIDED.
Patient problems: Insufficient Information
MAUDE report 19055688 ↗
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- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.