CARDINAL HEALTH SU130-1305 (UDI 10192253022339)Recalls & reported problems
Cardinal Health 200, LLC · JACKSON-PRATT 100CC BULB RESERVOIR · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253022339), received between Apr 17, 2026 and Apr 17, 2026 — classified as 1 malfunction.
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
Most reported problems
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 17, 2026
JACKSON PRATT DRAIN BULB NOT STAYING COMPRESSED AS DESIGNED. THE NURSE COMPRESSED THE BULB AND IT LOST SUCTION AND STOPPED WORKING AFTER ABOUT FIVE MINUTES. THE NURSE DECIDED TO SWITCH THE BULB AND WHEN THEY BEGAN THAT PROCESS, THE BULB'S CONNECTION TO THE TUBING WAS VERY LOOSE. THE NURSE REPLACED THE DEFECTIVE BULB WITH A NEW BULB AND THE DRAIN FUNCTIONED AS DESIGNED.
Patient problems: Insufficient Information
MAUDE report 24910243 ↗
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- 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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