Reported Apr 23, 2025 · Ongoing

Medline Convenience kits used for various procedures

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

Is this the product you have?

Medline Convenience kits used for various procedures

20 of 20 products

Products covered by this recall
Model / numberProduct as published
HCP075GANGIOGRAPHY DRAPE PACK
DYNJ64354AENSEMBLE CORONAROGRAPHIE-LF
0M-CP01029DRADIOL ANGIO PACK-LF
DYNJ81454BARTERIOGRAM PACK 2
DYNJ51338CCATH PACK
DYNDH1228BRISTOL MYELOGRAM
DYNJ83961ACARDIAC CATH-LEFT HEART
HCP075GANGIOGRAPHY DRAPE PACK
DYNJ85070CATH LAB PACK
DYNJ39515ACT SCAN PACK
00-398650AJANGIOGRAPHY DRAPE PACK
DYNJ24812DI.R. RADIOLOGY PACK
DYNJ69974(CH) ARTERIOGRAM ADD ON PACK
DYNJ69135ABASE HEMODYNAMIE-LF
DYNJ45020INTERVENTIONAL RADIOLOGY PACK
DYNJ51240APORTACATH PACK
DYNJ43969RADIOLOGY PACK
DYNJ41932ILEFT HEART SMGH-LF 2
0M-CP01029DRADIOL ANGIO PACK-LF
DYNJ81454BARTERIOGRAM PACK 2
Lot codes and dates

20 of 20 products

Products covered by this recall
#BarcodesProduct as published
11019532715631240195327156313Lot Number: 24IBS428; 2) DYNJ64354A, UDI-DI: 10195327156312(each), 40195327156313(case)
21088827785811440888277858115Lot Number: 24JBM450; 3) 0M-CP01029D, UDI-DI: 10888277858114(each), 40888277858115(case)
31019845910010940198459100100Lot Number: 24JBM593; 4) DYNJ81454B, UDI-DI: 10198459100109(each), 40198459100100(case)
41019348924171640193489241717Lot Number: 24JBN316; 5) DYNJ51338C, UDI-DI: 10193489241716(each), 40193489241717(case)
51088994257200740889942572008Lot Number: 24JBN784; 6) DYNDH1228, UDI-DI: 10889942572007(each), 40889942572008(case)
61019532751774840195327517749Lot Number: 24JBU509; 7) DYNJ83961A, UDI-DI: 10195327517748(each), 40195327517749(case)
71019845913445640198459134457Lot Number: 24JBW818; 8) HCP075G, UDI-DI: 10198459134456(each), 40198459134457(case)
81019532745539240195327455393Lot Number: 24JBX138; 9) DYNJ85070, UDI-DI: 10195327455392(each), 40195327455393(case)
91088994275313040889942753131Lot Number: 24JBY293; 10) DYNJ39515A, UDI-DI: 10889942753130(each), 40889942753131(case)
101019532733090340195327330904Lot Number: 24KBA200; 11) 00-398650AJ, UDI-DI: 10195327330903(each), 40195327330904(case)
111088438965321040884389653211Lot Number: 24KBA758; 12) DYNJ24812D, UDI-DI: 10884389653210(each), 40884389653211(case)
121019532700111740195327001118Lot Number: 24KBB397; 13) DYNJ69974, UDI-DI: 10195327001117(each), 40195327001118(case)
131019532714049640195327140497Lot Number: 24KBB454; 14) DYNJ69135A, UDI-DI: 10195327140496(each), 40195327140497(case)
141088827708668540888277086686Lot Number: 24KBC186; 15) DYNJ45020, UDI-DI: 10888277086685(each), 40888277086686(case)
151088994249352440889942493525Lot Number: 24KBC962; 16) DYNJ51240A, UDI-DI: 10889942493524(each), 40889942493525(case)
161088827707708940888277077080Lot Number: 24KBE652; 17) DYNJ43969, UDI-DI: 10888277077089(each), 40888277077080(case)
171019845907869940198459078690Lot Number: 24KBF965; 18) DYNJ41932I, UDI-DI: 10198459078699(each), 40198459078690(case)
181088827785811440888277858115Lot Number: 24KBG499; 19) 0M-CP01029D, UDI-DI: 10888277858114(each), 40888277858115(case)
191019845910010940198459100100Lot Number: 24KBG961; 20) DYNJ81454B, UDI-DI: 10198459100109(each), 40198459100100(case)
20Lot Number: 24KBH847
Amount recalled
4022 units

This recall covers 34 products

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

21 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

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.

Want the full recall guide?

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 Sep 19, 6:19 PM 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.