JACKSON-PRATT JP-2233Recalls & reported problems
Cardinal Health 200, LLC · JP CHAN DRN SIL HUBLES 15FR BND TRO · Class 1
All models of JACKSON-PRATT (20)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885380182655), received between Aug 23, 2022 and Aug 23, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Material Too Rigid or Stiff” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
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-0991-2023 · Root cause: Unknown/Undetermined by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Too Rigid or Stiff1
Patient problems
- Seroma1
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 23, 2022Material Too Rigid or Stiff; Material Too Rigid or Stiff
CUSTOMER REPORTED PHYSICIANS ARE HAVING ISSUES WITH THE DRAIN THAT IS ATTACHED TO A TROCAR, PASSING THROUGH THE SKIN. THE DRAIN IS STIFF AND HARD TO STRIP. DRAINAGE IS THEN LOW; THE DRAIN IS REMOVED, AND SEROMAS DEVELOP. AN ATTEMPT TO DRAIN THE SEROMA IS NOT ALWAYS SUCCESSFUL. THE PLASTICS GROUP RECENTLY HAD AN INFECTION. SEROMAS AFFECT THE ADHERENCE OF DERMAL TISSUE AND THE PHYSICAL APPEARANCE OF THE RECONSTRUCTIVE SURGERY. NO ADDITIONAL INFORMATION OR PATIENT DEMOGRAPHICS PROVIDED.
Patient problems: Seroma; Unspecified Infection
MAUDE report 15280447 ↗
Other CATHETER, IRRIGATION devices
- Navarre Opti-Drain NOD8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION901 reports
- Navarre NNU8LPTBard Access Systems, Inc. · CATHETER, IRRIGATION736 reports
- BLAKE 2227Ethicon Inc. · CATHETER, IRRIGATION331 reports
- Navarre NNU6LPTBard Access Systems, Inc. · CATHETER, IRRIGATION211 reports
- Navarre Opti-Drain NOD10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION178 reports
- Navarre NNU10LPTBard Access Systems, Inc. · CATHETER, IRRIGATION127 reports
- BLAKE 2233Ethicon Inc. · CATHETER, IRRIGATION114 reports
- Vasoshield VH-5001Maquet Cardiovascular LLC · Catheter, Irrigation1 recall27 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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