NA CB11Q27R1Recalls & reported problems
Medtronic, Inc. · CUSTOM PACK CB11Q27R1 MANIFOLD · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000703103), received between Jun 17, 2025 and Jun 17, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Crack” (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.
Reports received per month
Most reported problems
Device problems
- Crack1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 17, 2025Crack; Crack
IT WAS REPORTED THAT THERE WAS A CRACK IN THE MANIFOLD PORT OF THE CUSTOM TUBING PACKS DURING USE. A COMPLETE CRACK OR BREAK OCCURRED IN EACH CASE. THE DEVICES WERE REPLACED TO COMPLETE THE CASE. IT WAS UNKNOWN IF THERE WAS ANY PATIENT INVOLVEMENT OR COMPLICATIONS AS A RESULT OF THE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22223823 ↗
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-1894-2021 · Apr 29, 2021 · TerminatedMedtronic BB9G78R8, Custom Pack BB9G78R8 ECC Supp, Custom Perfusion System, Sterile, Rx.
- Z-1883-2021 · Apr 29, 2021 · TerminatedMedtronic HY10J00R12, Custom Pack HY10J00R12 ECC Small CA, Custom Perfusion System,
- Z-1882-2021 · Apr 29, 2021 · TerminatedMedtronic CB10W64R1, Custom Pack CB10W64R1 CH Access 3/8, Custom Perfusion System, Sterile, Rx.
- Z-1876-2021 · Apr 29, 2021 · TerminatedMedtronic CB7J97R8, Custom Pack CB7J97R8 U14 E Sup, Custom Perfusion System, Sterile, Rx.
- Z-1895-2021 · Apr 29, 2021 · TerminatedMedtronic 1A46R11, Custom Pack 1A46R11 Neonatal, Custom Perfusion System, Sterile, Rx.
- Z-1872-2021 · Apr 29, 2021 · TerminatedMedtronic HY8M63R4, Custom Pack HY8M63R4 Adult ECC, 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-1879-2021 · Apr 29, 2021 · TerminatedMedtronic CB10W63R1, Custom Pack CB10W63R1 HL 20 1/4, Custom Perfusion System, Sterile, Rx.
- Z-1873-2021 · Apr 29, 2021 · TerminatedMedtronic BB10R94R6, Custom Pack BB10R94R6 1/4 ECCPK, Custom Perfusion System, Sterile, Rx.
- Z-1893-2021 · Apr 29, 2021 · TerminatedMedtronic BB7D76R13, Custom Pack BB7D76R13 CORR HL, 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-1889-2021 · Apr 29, 2021 · TerminatedMedtronic CB7J98R7, Custom Pack CB7J98R7, Custom Pack CB7J98R7 3/8 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-1878-2021 · Apr 29, 2021 · TerminatedMedtronic CB1H18R20, Custom Pack CB1H18R20 Accesory, 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.
…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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