Reported Apr 23, 2025 · Ongoing

Medline Convenience kits used for various procedures: 1) ANGIO CONSOLIDATED PACK, Model Number: DYNJHTCAD1; 2)…

MEDLINE INDUSTRIES, LP - Northfield

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 - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753

Lot codes and dates: 3 of 3 products
Products covered by this recall
# Barcodes Product as published
1 1019348931662940193489316620 Lot Number: 24JBS743; 2) DYNJ05350V, UDI-DI: 10193489316629(each), 40193489316620(case)
2 1019348985491640193489854917 Lot Number: 24JBU500; 3) DYNJ38144C, UDI-DI: 10193489854916(each), 40193489854917(case)
3 Lot Number: 24KBD294
Amount recalled: 2,118 units

The agency filed one notice per product. You are reading one of them; the other 33 are below.

21 more are in the archive.

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

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

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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80 in total.

#	Barcodes	Product as published
1	`1019348931662940193489316620`	Lot Number: 24JBS743; 2) DYNJ05350V, UDI-DI: 10193489316629(each), 40193489316620(case)
2	`1019348985491640193489854917`	Lot Number: 24JBU500; 3) DYNJ38144C, UDI-DI: 10193489854916(each), 40193489854917(case)
3		Lot Number: 24KBD294