MAHURKAR 8888101004HPRecalls & reported problems
Mozarc Medical US LLC · Acute High Pressure Triple Lumen Catheter Tray,Curved Extensions with IC* Components · Class 2
All models of MAHURKAR (81)
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 10884521127982), received between Jun 26, 2019 and Jun 26, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Material Puncture/Hole” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
31 other recalls cover devices cleared under the same FDA submission (K102605, K192302); they may or may not involve this specific model.
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.
Recalls naming this device
- Jun 28, 2023Class IOpen, Classified
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An occluded, partially or fully, and/or uncured or excessive MDX may dislodge from the catheter lead to full catheter obstruction resulting in delay to treatment and partial obstruction resulting in reduced flow, or particulate dislodgement that may result in delay to treatment, hemolysis, embolism/embolus or thrombosis/thrombus
Z-2370-2023 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Puncture/Hole1
Patient problems
- Blood Loss1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 26, 2019Material Puncture/Hole; Material Puncture/Hole
ACCORDING TO THE REPORTER, PATIENT BEGAN BLEEDING FROM THE CATHETER WITH A CONCERN FOR A CRACK IN THE TUBING. THE PATIENT BLED A SIGNIFICANT AMOUNT (AMOUNT OF BLOOD LOSS WAS NOT KNOWN). IT WAS ALSO STATED THAT THE CRACK IN THE TUBING CAUSED THE BLEEDING, BUT THE PATIENT WAS ALREADY CRITICALLY ILL IN THE ICU GETTING CONTINUOUS DIALYSIS TREATMENTS. THE TUBING WAS SUCCESSFULLY CLAMPED OFF AND EXCHANGED THE LINE OVER A GUIDE WIRE. THE PATIENT IS STILL CRITICALLY ILL BUT STABLE IN THE ICU.
Patient problems: Blood Loss
MAUDE report 8733354 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K102605, K192302. One submission often covers many models, so check the product and lot details in each record.
- Z-0426-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Components: 12 Fr/Ch (4.0 mm) x 24 cm;
- Z-0422-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 16 cm;
- Z-0425-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
- Z-0424-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
- Z-0421-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 13 cm;
- Z-0423-2026 · Oct 17, 2025 · Open, ClassifiedMAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
- Z-2367-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, IC Tray REF:8888101001HP
- Z-2374-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
- Z-2381-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637HP
- Z-2369-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, IC Tray REF: 8888101003HP
- Z-2378-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629
- Z-2375-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, PASS Tray REF: 8888103004HP
- Z-2373-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, PASS Tray REF: 8888103001HP
- Z-2382-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions REF: 8888345512HP
- Z-2376-2023 · Jun 28, 2023 · Open, ClassifiedMAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, PASS Tray REF: 8888104003HP
…and 16 more.
Other CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED devices
- Power-Trialysis catheter 5605150Bard Access Systems, Inc. · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls13 reports
- Power-Trialysis catheter 5605240Bard Access Systems, Inc. · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls8 reports
- MAHURKAR 8888101002HPMozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls1 death8 reports
- Power-Trialysis Slim-Cath catheter 5855240Bard Access Systems, Inc. · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls4 reports
- Power-Trialysis catheter 5615200Bard Access Systems, Inc. · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls4 reports
- MAHURKAR 8888101003HPMozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls4 reports
- MAHURKAR 8888102003HPMozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls4 reports
- MAHURKAR 8888102004HPMozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED2 recalls3 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 · 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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