NA HY6V11R35Recalls & reported problems
Medtronic, Inc. · CUSTOM PACK HY6V11R35 AHC CB · Class 2
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 00763000402624), received between Jul 15, 2021 and Jul 15, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Misassembled During Installation” (1 report).
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.
Most reported problems
Device problems
- Misassembled During Installation1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2021Misassembled During Installation; Misassembled During Installation
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF THIS CUSTOM TUBING PACK DURING EXTRA CORPOREAL MEMBRANE OXYGENATION (ECMO), IT WAS NOTED THAT LUER CONNECTION SEPARATED FROM 1/8 TUBING THAT IT WAS ATTACHED TO. PERFUSION THEN REINSERTED THE TUBING ONTO THE LUER CONNECTION. PERFUSION THEN REPLACED THE 1/8 MALE LUER LINE WITH ANOTHER BACK UP LINE THEY HAD IN THIS PACK AND CONTINUED THE CASE. PATIENT IMPACT WAS REQUESTED BUT IT WILL NOT BE PROVIDED. BLOOD LOSS WAS MINIMAL ACCORDING TO THE HOSPITAL CONTACT (NO SPECIFIC AMOUNT WAS GIVEN). NO TRANSFUSION WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 12172110 ↗
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-1882-2021 · Apr 29, 2021 · TerminatedMedtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, 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-1891-2021 · Apr 29, 2021 · TerminatedMedtronic CB10Y89R10, Custom Pack CB10Y89R10 ECC 3/8 A/V, Custom Perfusion System, Sterile, Rx.
- Z-1871-2021 · Apr 29, 2021 · TerminatedMedtronic HY10Z48R2, Ctr., Custom Pack HY10Z48R2 Adult ECC 1/4, Custom Perfusion System, Sterile, Rx.
- Z-1892-2021 · Apr 29, 2021 · TerminatedMedtronic BB8M63R5, Custom Pack BB8M63R5 Adult ECC, Custom Perfusion system, Sterile, Rx.
- Z-1877-2021 · Apr 29, 2021 · TerminatedMedtronic HY11B40R1, Custom Pack HY11B40R1 1/4 Respirato, Custom Perfusion System, Sterile, Rx.
- Z-1878-2021 · Apr 29, 2021 · TerminatedMedtronic CB1H18R20, Custom Pack CB1H18R20 Accesory, Custom Perfusion System, Sterile, Rx.
- Z-1874-2021 · Apr 29, 2021 · TerminatedMedtronic BB11J14R2, Custom Pack BB11J14R2 Bridge, Custom Perfusion System, Sterile, Rx.
- Z-1881-2021 · Apr 29, 2021 · TerminatedMedtronic CB4W67R20, Custom Pack CB4W67R20 Adult E, Custom Perfusion System, Sterile, Rx.
- Z-1872-2021 · Apr 29, 2021 · TerminatedMedtronic HY8M63R4, Custom Pack HY8M63R4 Adult ECC, Custom Perfusion System, Sterile, Rx.
- Z-1880-2021 · Apr 29, 2021 · TerminatedMedtronic HY8R62R13,Custom Pack HY8R62R13 E Pack, 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-1893-2021 · Apr 29, 2021 · TerminatedMedtronic BB7D76R13, Custom Pack BB7D76R13 CORR HL, 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.
…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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