CARDINAL HEALTH SU130-1360Recalls & reported problems
Cardinal Health 200, LLC · KIT DRAIN 100CC W/7MM PERF · Class 1 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10192253022537), received between May 7, 2022 and May 16, 2023 — classified as 1 injury, 1 malfunction.
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
- Difficult to Remove1
- Fracture1
Patient problems
- Foreign Body In Patient1
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 16, 2023Break; Break
CUSTOMER REPORTED THAT THE SPINE SURGEON TRIED TO PLACE A JP DRAIN AND WHEN HE GRABBED THE END TO PULL IT THROUGH THE INCISION, THE PLASTIC LITERALLY CRUMBLED. PIECE WAS RETRIEVED WITH NO ADVERSE EFFECT TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16942850 ↗InjuryMay 7, 2022Break; Fracture; Difficult to Remove; Fracture
PER CUSTOMER, HEALTH CARE PROFESSIONAL WAS ASKED TO ASSIST WITH REMOVING A JACKSON PRATT DRAIN FROM PATIENT'S LOWER ABDOMEN. IT WAS CONFIRMED THAT DRAIN TO THE RIGHT OF HER LOWER ABDOMEN HORIZONTAL INCISION HAD THE SUTURE SECURING THE DRAIN REMOVED ALREADY. HEALTH CARE PROFESSIONAL EXPLAINED THE PROCEDURE TO THE PATIENT AND BEGAN PULLING ON THE JP DRAIN WITH THE USUAL AMOUNT OF FORCE. JP DRAIN WAS NOT COMING OUT EASILY. MODERATE RESISTANCE FELT. HEALTH CARE PROFESSIONAL REPOSITIONED HAND ON DRAIN CLOSER TO INSERTION SITE AND BEGAN TO PULL WITH MODERATE FORCE WHEN DRAIN BROKE AND RETRACTED BACK INTO INSERTION SITE. HEALTH CARE PROFESSIONAL DID NOT USE EXCESSIVE FORCE AND HAS SUCCESSFULLY REMOVED JP DRAINS WITH THE SAME AMOUNT OF MODERATE FORCE ON OTHER PATIENTS BEFORE. HEALTH CARE PROFESSIONAL WAS VERY SURPRISED THAT DRAIN BROKE WITH THAT AMOUNT OF FORCE. EITHER DRAIN TUBING IS REPORTEDLY DEFECTIVE AND BROKE WITH MODERATE FORCE OR PERHAPS THE DRAIN WAS SUTURED INSIDE THE ABDOMEN ACCIDENTLY DURING PRIOR EMERGENCY SURGERY AND WAS COMPROMISED BY A SUTURE. PATIENT TO GO BACK FOR SURGERY TO OPEN THE LOWER ABDOMINAL WOUND TO RETRIEVE THE REMAINING PIECE OF DRAIN FROM THE PATIENT'S ABDOMEN
Patient problems: Foreign Body In Patient; Insufficient Information
MAUDE report 14316003 ↗
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- Closed Wound Suction 0034610C. R. Bard, Inc. · APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED62 reports
- CARDINAL HEALTH SU130-402DCardinal Health 200, LLC · APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED1 recall1 report
- CARDINAL HEALTH SU130-475Cardinal Health 200, LLC · APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED1 recall0 reports
- CARDINAL HEALTH SU130-403DCardinal Health 200, LLC · APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED1 recall0 reports
- NA 1A8504Baxter International Inc. · APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED50 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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