Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026

1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV SHUNT PACK-MARYVIEW, Medline…

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

64 of 64 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ911589A1019845964610240198459646103Medline product number/ , UDI/DI 10198459646102 (each) 40198459646103 (case), Lot Number 26CBD487
DYNJ9117101019845951570540198459515706Medline product number/ , UDI/DI 10198459515705 (each) 40198459515706 (case), Lot Number 26BLA622
DYNJ35312K1019845931157440198459311575Medline product number/ , UDI/DI 10198459311574 (each) 40198459311575 (case), Lot Number 26ADA368
DYNJT76071019845963947040198459639471Medline product number/ , UDI/DI 10198459639470 (each) 40198459639471 (case), Lot Number 26ABP608
DYNJ9117101019845951570540198459515706Medline product number/ , UDI/DI 10198459515705 (each) 40198459515706 (case), Lot Number 25KLA755
DYNJ35312K1019845931157440198459311575Medline product number/ , UDI/DI 10198459311574 (each) 40198459311575 (case), Lot Number 25KDA055
DYNJ9117101019845951570540198459515706Medline product number/ , UDI/DI 10198459515705 (each) 40198459515706 (case), Lot Number 25JLA081
DYNJ80549D1019845938961040198459389611Medline product number/ , UDI/DI 10198459389610 (each) 40198459389611 (case), Lot Number 25JBQ932
DYNJ35312K1019845931157440198459311575Medline product number/ , UDI/DI 10198459311574 (each) 40198459311575 (case), Lot Number 25IDA242
DYNJ80549D1019845938961040198459389611Medline product number/ , UDI/DI 10198459389610 (each) 40198459389611 (case), Lot Number 25HBV035
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 25ELA868
DYNJ35312K1019845931157440198459311575Medline product number/ , UDI/DI 10198459311574 (each) 40198459311575 (case), Lot Number 25EDA603
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 25BLA807
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 25BLA545
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 25ALA107
DYNJ35312J1019532720981040195327209811Medline product number/ , UDI/DI 10195327209810 (each) 40195327209811 (case), Lot Number 24LDA717
DYNJ35312J1019532720981040195327209811Medline product number/ , UDI/DI 10195327209810 (each) 40195327209811 (case), Lot Number 24LDA627
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 24KLA675
DYNJ908879C1019532769088540195327690886Medline product number/ , UDI/DI 10195327690885 (each) 40195327690886 (case), Lot Number 24KBD462
DYNJ24528P1019845912953740198459129538Medline product number/ , UDI/DI 10198459129537 (each) 40198459129538 (case), Lot Number 24JLA497
Amount recalled
1834 kits

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

  • Nationwide

Why it was recalled

Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 1:07 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.