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Groshong 7741700Recalls & reported problems

Bard Access Systems, Inc. · Groshong CV Catheter Repair Kit for Use with Groshong 7F Single-Lumen CV Catheter · Class 2

All models of Groshong (12)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741037726), received between Dec 21, 2018 and Dec 21, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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.

Most reported problems

Device problems

  • Fluid/Blood Leak1

Patient problems

  • Fever1
  • No Consequences Or Impact To Patient1
  • Unspecified Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 21, 2018Fluid/Blood Leak; Fluid/Blood Leak

    IT WAS REPORTED THAT AFTER THE CENTRAL VENOUS CATHETER WAS REPAIRED, IT ALLEGEDLY LEAKED. THERE WAS NO REPORTED PATIENT INJURY.

    Patient problems: Fever; No Consequences Or Impact To Patient; Unspecified Infection

    MAUDE report 8189675 ↗

Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices

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Sources and updates

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