JACKSON-PRATT JP-2212Recalls & reported problems
Cardinal Health 200, LLC · JP CHAN DRN SIL FLT 7MM FULL 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
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885380182495), received between May 10, 2023 and Jan 12, 2024 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (3 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-0975-2023 · Root cause: Unknown/Undetermined by firm · FDA record ↗
Most reported problems
Device problems
- Break3
Patient problems
- Insufficient Information2
- Foreign Body In Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 12, 2024Break; Break
MW5148639: THE NEURO APRN(ADVANCED REGISTERED NURSE PRACTITIONER) ATTEMPTED TO REMOVE THE JP (JACKSON-PRATT) DRAIN WHICH BROKE AT THE INSERTION SITE AND A DRAIN FRAGMENT REMAINED IN THE PATIENT. THE NEUROSURGEON ATTEMPTED TO REMOVE THE FRAGMENT AT THE BEDSIDE WITHOUT SUCCESS. THE PT RETURNED TO THE OR(OPERATING ROOM) FOR SURGICAL REMOVAL OF THE JP DRAIN FRAGMENT.
Patient problems: Foreign Body In Patient
MAUDE report 18505281 ↗MalfunctionMay 19, 2023Break; Break
CUSTOMER REPORTED THAT DURING REMOVAL OF JP DRAIN FROM THE PATIENT, IT BROKE. THIS IS 1 OF 3 EVENTS THAT HAS HAPPENED AT OUR INSTITUTION WITH THE SAME DRAIN. EVENT DATE IS UNKNOWN. NO FURTHER INFORMATION WAS PROVIDED WHEN REQUESTED.
Patient problems: Insufficient Information
MAUDE report 16969507 ↗MalfunctionMay 10, 2023Break; Break
DURING REMOVAL OF JP DRAIN FROM THE PATIENT'S SCALP, THE JUNCTION BETWEEN THE CLEAR DRAIN TUBING AND FLUTED WHITE PIECE APPEARED TO BE SEVERED AND EMERGED FROM SCALP, LEAVING THE LENGTH OF THE SUBGALEAL PORTION RETAINED IN THE WOUND. THIS IS THE 3RD EVENT THAT THIS HAS HAPPENED AT OUR INSTITUTION WITH THE SAME DRAIN. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Insufficient Information
MAUDE report 16907876 ↗
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- Navarre NNU10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION127 reports
- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
- Vasoshield VH-5001Maquet Cardiovascular LLC · Catheter, Irrigation1 recall27 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.