NA HY11F32R4Recalls & reported problems
Medtronic, Inc. · CUSTOM PACK HY11F32R4 ACCESSORY 1/4 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00763000630218), received between Jan 17, 2023 and Apr 11, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (3 reports).
25 other recalls cover devices cleared under the same FDA submission (K171979); 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak3
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.
MalfunctionApr 11, 2024Fluid/Blood Leak; Fluid/Blood Leak
MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A CUSTOM PACK, THE CUSTOM OBSERVED A LEAK INSIDE THE TABLE TRAY AT THE QUICK CONNECTIONS. THE CUSTOMER STATED THAT WHEN THIS HAPPENS THEY CAN NOT BE CERTAIN OF STERILITY AND CAN NOT BLOOD PRIME THE CIRCUIT BECAUSE IT WOULD MAKE TOO BIG OF A MESS. THERE WAS NO PACKAGE DAMAGE NOTED AND THE CUSTOMER HAS DECIDED TO REMOVE THE QUICK CONNECTS FROM THE CIRCUIT TO AVOID THIS ISSUE IN THE FUTURE. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19086081 ↗MalfunctionOct 9, 2023Fluid/Blood Leak; Fluid/Blood Leak
MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A CUSTOM TUBING PACK, IT WAS REPORTED THAT A LEAK WAS DISCOVERED INSIDE THE TABLE TRAY. IT WAS NOT CLEAR WHERE THE LEAK WAS COMING FROM. THE CUSTOMER STATED THAT IT WAS POSSIBLY FROM ONE OF THE QUICK CONNECTORS. THE CIRCUIT WAS NEVER USED FOR A PATIENT AND WAS SET ASIDE FOR RETURN. NO PACKAGE DAMAGE WAS NOTED DURING INITIAL SETUP. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THERE WAS NO VISIBLE BREAK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17894462 ↗MalfunctionJan 17, 2023Fluid/Blood Leak; Fluid/Blood Leak
MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A CUSTOM TUBING PACK, IT WAS REPORTED THAT THE CUSTOM PACK HAD A LEAK WHILE PRIMING. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THERE WAS NO DAMAGE TO THE PACKAGING. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE LEAK DID NOT APPEAR IN MULTIPLE PACKS. THE LEAK WAS FROM THE LINE 1 OF THE CUSTOM TUBING PACK SPECIFICATION INSIDE THE TABLE TRAY. THERE WAS NO VISIBLE AIR IN THE SYSTEM/TUBING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16181542 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K171979. One submission often covers many models, so check the product and lot details in each record.
- Z-1879-2021 · Apr 29, 2021 · TerminatedMedtronic CB10W63R1, Custom Pack CB10W63R1 HL 20 1/4, Custom Perfusion System, Sterile, Rx.
- Z-1884-2021 · Apr 29, 2021 · TerminatedMedtronic CB10W65R1, Custom Pack CB10W65R1 CH Access1/4, Custom Perfusion System, Sterile, Rx.
- Z-1888-2021 · Apr 29, 2021 · TerminatedMedtronic CB10R55R5, Custom Pack CB10R55R5 3/8X3/8 Loop, Custom Perfusion System, Sterile, Rx.
- Z-1887-2021 · Apr 29, 2021 · TerminatedMedtronic CB10R79R6, Custom Pack CB10R79R6 1/4X1/4 Loop, Custom Perfusion System, Sterile, Rx.
- Z-1890-2021 · Apr 29, 2021 · TerminatedMedtronic HY10L28R3, Custom Pack HY10L28R3 1/4 Pack, Custom Perfusion System, Sterile, Rx.
- Z-1886-2021 · Apr 29, 2021 · TerminatedMedtronic HY10D90R2, Custom Pack HY10D90R2 3/8 ACC, Custom Perfusion System, Sterile, Rx.
- Z-1875-2021 · Apr 29, 2021 · TerminatedMedtronic HY7M07R6, Custom Pack HY7M07R6 E 1/4, Custom Perfusion System, Sterile, Rx.
- Z-1885-2021 · Apr 29, 2021 · TerminatedMedtronic HY10Y54R4, Custom Pack HY10Y54R4 ECC PED 1/4, Custom Perfusion System, Sterile, Rx.
- Z-1893-2021 · Apr 29, 2021 · TerminatedMedtronic BB7D76R13, Custom Pack BB7D76R13 CORR HL, Custom Perfusion System, Sterile, Rx.
- Z-1883-2021 · Apr 29, 2021 · TerminatedMedtronic HY10J00R12, Custom Pack HY10J00R12 ECC Small CA, Custom Perfusion System,
- Z-1880-2021 · Apr 29, 2021 · TerminatedMedtronic HY8R62R13,Custom Pack HY8R62R13 E Pack, Custom Perfusion System, Sterile, Rx.
- Z-1894-2021 · Apr 29, 2021 · TerminatedMedtronic BB9G78R8, Custom Pack BB9G78R8 ECC Supp, Custom Perfusion System, Sterile, Rx.
- Z-1889-2021 · Apr 29, 2021 · TerminatedMedtronic CB7J98R7, Custom Pack CB7J98R7, Custom Pack CB7J98R7 3/8 Pack, Custom Perfusion System, Sterile, Rx.
- Z-1872-2021 · Apr 29, 2021 · TerminatedMedtronic HY8M63R4, Custom Pack HY8M63R4 Adult ECC, Custom Perfusion System, Sterile, Rx.
- Z-1878-2021 · Apr 29, 2021 · TerminatedMedtronic CB1H18R20, Custom Pack CB1H18R20 Accesory, Custom Perfusion System, Sterile, Rx.
…and 10 more.
Other Catheter, cannula and tubing, vascular, cardiopulmonary bypass devices
- DLP™ 77010Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass1 recall154 reports
- EOPA™ 77422Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls19 reports
- DLP™ 77008Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls9 reports
- NA HY11W65R1Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls8 reports
- DLP® 12113Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls6 reports
- DLP® Aortic Root Cannula with Flow-Guard™ 11012Medtronic, Inc. · CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS2 recalls5 reports
- EOPA™ 77622Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls4 reports
- NA HY11R00R6Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 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
- 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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