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Dover 6156MFRecalls & reported problems

Cardinal Health, Inc. · True content to be populated as part of rebranding · Class 2

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10192253059809), received between Jul 13, 2022 and Jul 13, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Obstruction of Flow” (3 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Obstruction of Flow3

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 13, 2022Obstruction of Flow; Obstruction of Flow

    THE CUSTOMER REPORTED THAT THE URINE ACCUMULATED AT THE CONNECTION BETWEEN THE RUNNING TUBE AND THE BAG AND DID NOT FLOW. THEY DRAINED THE URINE IN THE BAG AND PINCHED THE CHAMBER PART OF THE CONNECTION BETWEEN THE BAG AND RUNNING TUBE, AND ALTHOUGH IT MAY HAVE FLOWED A LITTLE, THEY REPLACED IT. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15002206 ↗
  • MalfunctionJul 13, 2022Obstruction of Flow; Obstruction of Flow

    THE CUSTOMER REPORTED THAT THE URINE ACCUMULATED AT THE CONNECTION BETWEEN THE RUNNING TUBE AND THE BAG AND DID NOT FLOW. THEY DRAINED THE URINE IN THE BAG AND PINCHED THE CHAMBER PART OF THE CONNECTION BETWEEN THE BAG AND RUNNING TUBE, AND ALTHOUGH IT MAY HAVE FLOWED A LITTLE, THEY REPLACED IT. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15002159 ↗
  • MalfunctionJul 13, 2022Obstruction of Flow; Obstruction of Flow

    THE CUSTOMER REPORTED THAT THE URINE ACCUMULATED AT THE CONNECTION BETWEEN THE RUNNING TUBE AND THE BAG AND DID NOT FLOW. THEY DRAINED THE URINE IN THE BAG AND PINCHED THE CHAMBER PART OF THE CONNECTION BETWEEN THE BAG AND RUNNING TUBE, AND ALTHOUGH IT MAY HAVE FLOWED A LITTLE, THEY REPLACED IT. THERE WAS NO PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15002118 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.