Cardiothoracic Adaptor 072510Recalls & reported problems
C. R. Bard, Inc. · Cardiothoracic Adaptor · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741050046), received between Nov 15, 2018 and Sep 4, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Disconnection” (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. 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
- Disconnection3
- Detachment of Device or Device Component1
- Device Slipped1
- Nonstandard Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient2
- Discomfort1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2026Disconnection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50620019 ↗MalfunctionJul 22, 2024Disconnection; Disconnection
IT WAS REPORTED THAT CUSTOMER HAS SOME ISSUES WITH ONE OF THE WOUND DRAINAGE ACCESSORIES. THE BELOW ITEM WAS LISTED AS COMPARABLE TO THE BCC1 AND BCC2 FROM ETHICON, BUT OUR CVOR AREA WAS ADVISING THAT THE CAPS DO NOT STAY ON THE NEW BARD MEDICAL. THESE CAPS WILL NOT PROVIDE A TIGHT SEAL AND CAN COME OFF. ITEM 072510 WAS AN EXACT CROSS FOR BCC3 ,3 IN 1 CONNECTOR BUT WAS NOT A LIKE FOR LIKE FOR THE OTHER TWO, BCC1 AND BCC2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19793305 ↗MalfunctionDec 5, 2019Nonstandard Device; Nonstandard Device; Device Slipped
IT WAS REPORTED THAT ADDITIONAL PORTS WERE ACCIDENTALLY OPENING, AND THE BULKINESS OF THE DRAIN CAUSED DISCOMFORT. HEALTH PROFESSIONAL STATED THEY WERE CONCERNED THAT THE BULKINESS COULD CAUSE SKIN BREAKDOWN POST CARDIAC SURGERY.
Patient problems: Discomfort; No Consequences Or Impact To Patient
MAUDE report 9416523 ↗MalfunctionNov 15, 2018Disconnection; Disconnection; Detachment of Device or Device Component
IT WAS REPORTED THAT TWO OF THE PORTS OF THE 3-IN-1 DRAIN CONNECTOR BECAME UNPLUGGED DURING USE, WHICH INTRODUCED AIR INTO THE THORACIC CAVITY. THERE WAS NO REPORTED INJURY TO THE PATIENT, HOWEVER THE COMPLAINANT NOTED THAT THERE WAS A RISK OF RESPIRATORY COMPROMISE. THE CONNECTOR WAS BEING USED WITH A SINGLE DRAIN, SO THE PORTS THAT BECAME DISCONNECTED WERE NOT IN USE.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 8075796 ↗
Other ADAPTOR, CATHETER devices
- Spray Catheter WP-18/2200Micro-Tech (Nanjing) Co., Ltd. · Adaptor, Catheter8 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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