Hohn Catheter for Central Venous Placement 6600730Recalls & reported problems
Bard Access Systems, Inc. · Hohn Percutaneous 7F Dual-Lumen Catheter Basic Kit · Class 2 · Implant
All models of Hohn Catheter for Central Venous Placement (3)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 16
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 00801741036705), received between Jul 12, 2019 and Aug 5, 2021 — classified as 16 malfunctions.
The most frequently reported specific device problem is “Material Rupture” (5 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
- Material Rupture5
- Fluid/Blood Leak4
- Material Puncture/Hole4
- Crack3
- Device Markings/Labelling Problem2
- Adverse Event Without Identified Device or Use Problem1
- Material Split, Cut or Torn1
- Obstruction of Flow1
Patient problems
- No Known Impact Or Consequence To Patient8
- No Consequences Or Impact To Patient4
- No Clinical Signs, Symptoms or Conditions2
- Perforation1
- Tissue Damage1
Recent adverse event reports
The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 5, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED VIA PHONE CALL "THAT THEY HAVE ORDERED HOHN¿ CENTRAL VENOUS CATHETERS REF#6600730, (2 EACH) AND THE SIZE IS NOT AS LISTED ON BD WEBSITE WHICH IS 42CM LENGTH INSTEAD SHE GOT 24CM LENGTH." THIS REPORT ADDRESSES THE SECOND OF TWO CATHETERS RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12282143 ↗MalfunctionAug 5, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED VIA PHONE CALL "THAT THEY HAVE ORDERED HOHN® CENTRAL VENOUS CATHETERS REF#6600730, (2 EACH) AND THE SIZE IS NOT AS LISTED ON BD WEBSITE WHICH IS 42CM LENGTH INSTEAD SHE GOT 24CM LENGTH." THIS REPORT ADDRESSES THE FIRST OF TWO CATHETERS RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12282128 ↗MalfunctionMar 12, 2020Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED PER RECEIVED MEDWATCH, "A HOLE WAS NOTICED IN THE HOHN CATHETER".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9823736 ↗MalfunctionMar 12, 2020Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED PER RECEIVED MEDWATCH, "CATHETER LEAKING UPON INJECTION OF ONE LUMEN".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9823734 ↗MalfunctionMar 12, 2020Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED PER RECEIVED MEDWATCH "THERE WAS A VISIBLE HOLE ON THE OUTSIDE OF THE CATHETER. THE DEVICE WAS EXCHANGED FOR A NEW HOHN CATHETER".
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9823418 ↗MalfunctionOct 23, 2019Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED VIA MEDWATCH, "DURING FLUSHING THE HOHN CATHETER WAS DAMAGED."
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9224653 ↗MalfunctionJul 12, 2019Material Puncture/Hole; Material Rupture
IT WAS REPORTED THE LUMEN ON PATIENT'S DOUBLE LUMEN NON-TUNNELED RIGHT IJ BURST, HOLE FORMED WHEN FLUSHED BETWEEN INSERTION SITE AND LUER LOCK. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786335 ↗MalfunctionJul 12, 2019Crack; Material Rupture; Obstruction of Flow
IT WAS REPORTED THAT THE CATHETER RUPTURING EXTERNAL LUMEN/CRACKING OR UPON FLUSHING. NO OTHER INFORMATION WAS PROVIDED. ON 7/10/2019: ADDT'L INFORMATION REC'D VIA MEDWATCH: "HOHN LINE FOUND TO HAVE ONE LUMEN W/ OBSTRUCTION EARLY MORNING, CONCERN FOR CLOT. HEPARIN WAS ORDERED TO CLEAR LINE. ON FLUSHING, MINIMAL PRESSURE WAS APPLIED BY PATIENT NURSE W/ SUBSEQUENT RUPTURE OF THE EXTERNAL PORTION OF ONE OF THE LUMENS OF THE LINE. RUPTURED LUMEN WAS CLAMPED BETWEEN THE RUPTURE AND THE PATIENT TO ENSURE NO FREE AIR ENTERED THE LINE. ENTERED AS PATIENT HARM DUE TO PATIENT REQUIRING ADDITIONAL PERIPHERAL IV PLACED W/ NEED FOR HOHN REPLACEMENT. PATIENT W/ NO ADVERSE EFFECTS OTHERWISE AT THIS TIME."
Patient problems: Tissue Damage
MAUDE report 8786328 ↗MalfunctionJul 12, 2019Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THE HOLE PERFORATED IN THE LUMEN PAST THE CLAMP SITE. NO OTHER INFORMATION PROVIDED.
Patient problems: Perforation
MAUDE report 8786093 ↗MalfunctionJul 12, 2019Material Rupture
IT WAS REPORTED THAT DURING FLUSH WHITE SALINE, WHITE LUMEN BUSTED. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786091 ↗MalfunctionJul 12, 2019Material Puncture/Hole
IT WAS REPORTED UPON FLUSHING RED LUMEN ON DOUBLE LUMEN HOHN, A HOLE POPPED OPEN ON LUMEN. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786089 ↗MalfunctionJul 12, 2019Material Split, Cut or Torn
IT WAS REPORTED THE RED HOHN LINE SPLIT DURING CONTRAST INJECTION. NO OTHER INFORMATION PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786088 ↗MalfunctionJul 12, 2019Material Puncture/Hole
IT WAS REPORTED THE FLUSHING OF THE CATHETER CAUSED A PERFORATION THAT FORMED A HOLE. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786086 ↗MalfunctionJul 12, 2019Material Puncture/Hole
IT WAS REPORTED UPON FLUSHING RED PORT NOTICED HOLE IN LINE WHILE FLUSHING. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8786083 ↗MalfunctionJul 12, 2019Crack; Material Rupture
IT WAS REPORTED THAT THE CATHETER RUPTURING EXTERNAL LUMEN/CRACKING OR UPON FLUSHING. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8785992 ↗MalfunctionJul 12, 2019Crack; Material Rupture
IT WAS REPORTED THAT THE CATHETER RUPTURING EXTERNAL LUMEN/CRACKING OR UPON FLUSHING. THE ORIGINAL HOHN WAS PLACED (B)(6) 2019.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8785807 ↗
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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
- 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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