CARDINAL HEALTH SU130-402D (UDI 10192253016420)Recalls & reported problems
Cardinal Health 200, LLC · JP 3-SPRING RES W/10FR PVC DRAIN/TR · Class 1 · Implant
Data updated Oct 18, 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 10192253016420), received between Jan 11, 2024 and Jan 11, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Recalls naming this device
- Mar 27, 2024Class IIOpen, Classified
Cardinal Health is issuing a lot number specific voluntary removal of Jackson-Pratt 3-Spring Reservoir kits due to specific products being shipped to users before undergoing sterilization.
Z-1736-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 11, 2024Break; Break
WHEN REMOVING A HEMOVAC DRAIN AT THE BEDSIDE (DRAIN WAS PLACED IN THE OPERATING ROOM), PART OF THE TUBING BROKE OFF AND WAS RETAINED WITHIN THE PATIENT. OTHER INFORMATION ABOUT THE PATIENT THAT MAY HAVE INFLUENCED THE OUTCOME OF THE EVENT: PLACEMENT OF FOUR DRAINS WAS RUSHED DUE TO EMERGENT AND CRITICAL NATURE OF PATIENT'S PROCEDURES. PATIENT HAS MASSIVE SPINAL TRAUMA AND HAD FOUR DRAINS PLACED IN HIS BACK, DURING PROCEDURE IT WAS RUSHED IN ORDER TO GET THE PATIENT ON THEIR BACK, INSTEAD OF ON THEIR STOMACH WHILE THEY OPERATED ON PATIENT'S SPINE, IN CASE COMPRESSIONS WERE NEEDED.
Patient problems: Foreign Body In Patient
MAUDE report 18492255 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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