JACKSON-PRATT JP-2211 (UDI 00885380020493)Recalls & reported problems
Cardinal Health 200, LLC · JP CHANNEL DRAIN 7MM, FULL FLUTES · Class 1
All models of JACKSON-PRATT (20)
Data updated Oct 16, 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 00885380020493), received between Jun 9, 2025 and Jun 9, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Entrapment of Device” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Entrapment of Device1
- Retraction Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 9, 2025Entrapment of Device; Retraction Problem
1315 PAGED PA [PHYSICIAN ASSISTANT], TO INFORM UPON REMOVAL OF JP [JACKSON-PRATT] DRAIN SOME RESISTANCE NOTICE. DRAIN SEEMS EMBEDDED INSIDE THE SKIN. RN, AT BEDSIDE ASSES, TRY TO RETRIEVE THE DRAIN AND UNABLE TO DO SO. STOP ANY ADDITIONAL ATTEMPT. PLACE A NEW DRESSING. PT AWARE OF SITUATION, NO DISTRESS NOTED. INFORM CHARGE NURSE, AND PRIMARY RN OF CURRENT SITUATION. 1325 PAGED DR. REGARDING NOT BEING ABLE TO REMOVE JP DRAIN. AWARE NO, NEW ORDERS AT THIS TIME 1345 PAGED AGAIN, PA FOR NEW ORDERS. AWAITING RESPONSE. 1400 PAGED ALTERNATE PA, INFORM HIM REGARDING THE JP DRAIN SITUATION. PER PA, WILL COME TO ASSESS AT BEDSIDE. 1417 PA AT BEDSIDE. 1445 BEDSIDE STERILE PROCEDURE, PERFORMED BY PA. SUCCESSFULLY REMOVE JP DRAIN, NO RETRAIN OBJECT. PT TOLERATED WELL. ASSES AND CHANGE SURGICAL SITE. PT STATED PAIN 10/10, DILAUDID GIVEN PER ORDER. 1500 PER PA, IS OKAY TO CONTINUE WITH DISCHARGE.
Patient problems: Pain
MAUDE report 22166194 ↗
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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