JACKSON-PRATT JP-2214Recalls & reported problems
Cardinal Health 200, LLC · JP CHANNEL DRAIN 10MM, FULL FLUTES · 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
- 3
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885380182518), received between Oct 18, 2023 and Feb 28, 2024 — classified as 3 injuries.
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-0977-2023 · Root cause: Unknown/Undetermined by firm · FDA record ↗
Most reported problems
Device problems
- Break3
Patient problems
- Foreign Body In Patient3
- Insufficient Information2
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryFeb 28, 2024Break; Break
CUSTOMER REPORTED THEY HAD TWO INCIDENTS NOW THAT WHEN REMOVING THE DRAIN A PIECE BREAKS OFF AND STAYS IN THE PATIENT AND THEY HAVE TO RETURN TO SURGERY FOR REMOVAL. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Foreign Body In Patient; Insufficient Information
MAUDE report 18803262 ↗InjuryFeb 28, 2024Break; Break
CUSTOMER REPORTED THEY HAD TWO INCIDENTS NOW THAT WHEN REMOVING THE DRAIN A PIECE BREAKS OFF AND STAYS IN THE PATIENT AND THEY HAVE TO RETURN TO SURGERY FOR REMOVAL. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Foreign Body In Patient; Insufficient Information
MAUDE report 18803254 ↗InjuryOct 18, 2023Break; Break
THE DRAIN TUBE BROKE WHEN THE SURGEON WAS REMOVING IT FROM THE PATIENT. IT LEFT ABOUT A 5" PIECE INSIDE THE PATIENT REQUIRING PATIENT TO BE RETURNED TO SURGERY FOR REMOVAL. THE PATIENT WAS RETURNED TO SURGERY FOR REMOVAL AND ADMINISTERED MEDICATION FOR ANESTHESIA AND RECOVERY. HE WAS DISCHARGED IN STABLE CONDITION TO SKILLED NURSING.
Patient problems: Foreign Body In Patient
MAUDE report 17961686 ↗
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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.