CARDINAL HEALTH SU130-1310 (UDI 10885380064029)Recalls & reported problems
Cardinal Health 200, LLC · JP PERF DRN SIL FLT 7MM FULL · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10885380064029), received between Jun 13, 2017 and Feb 13, 2020 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
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 18, 2026.
Most reported problems
Device problems
- Break2
- Adverse Event Without Identified Device or Use Problem1
- Detachment Of Device Component1
- Detachment of Device or Device Component1
Patient problems
- No Code Available1
- No Known Impact Or Consequence To Patient1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 13, 2020Break; Detachment of Device or Device Component
CUSTOMER REPORTED THAT WHILE REMOVING A JACKSON PRATT DRAIN IN ORDER TO PLACE A PICO DRESSING ON PATIENT¿S RIGHT KNEE, THE DRAIN PARTIALLY BROKE OFF INSIDE OF THE PATIENT¿S KNEE. THERE WAS REPORTEDLY LITTLE RESISTANCE WITH REMOVAL OF DRAIN. PATIENT WAS TAKEN BACK TO THE OR TO ENSURE BROKEN PIECES WERE REMOVED.
Patient problems: No Code Available
MAUDE report 9708502 ↗MalfunctionJun 23, 2018Break; Detachment Of Device Component
PATIENT CAME POST-OP WITH JP IN "BACK" INCISION. NURSING ATTEMPTED TO DISCONNECT DRAIN WHEN ORDERED. NURSE REPORTED USING USUAL METHOD OF REMOVAL AND FEELING NO UNUSUAL AMOUNT OF RESISTANCE. DRAIN BROKE OFF AT INSERTION SITE AND SURGEON HAD TO OPEN INCISION TO REMOVE REST OF DRAIN MANUALLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7632453 ↗InjuryJun 13, 2017Adverse Event Without Identified Device or Use Problem
OUR CUSTOMER, (B)(6), RECEIVED A VOICEMAIL MESSAGES FROM AN ATTORNEY CALLING ON BEHALF OF A FEMALE PATIENT OF DR.(B)(6)'S OFFICE. HE INDICATED THE JACKSON PRATT 7MM FLAT DRAIN FULL PERF CATALOG NUMBER SU130-1310 WAS USED ON HIS CLIENT PRIOR TO THE PRODUCT BEING RECALLED AND THE PATIENT WAS INFECTED AND HAD SPENT FOUR DAYS IN THE HOSPITAL. BEYOND THAT, HE IS NOT CERTAIN WHAT OTHER PERMANENT INJURIES THERE MAY BE. THE DATE OF INCIDENT AND PATIENT'S AGE WAS NOT PROVIDED. THIS IS ALL THE INFORMATION WE HAVE AT THIS TIME RELATED TO THIS EVENT.
Patient problems: Unspecified Infection
MAUDE report 6638734 ↗
Other CATHETER, IRRIGATION devices
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- 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
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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