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
| Model / number | Product as published |
|---|---|
HCP075G | ANGIOGRAPHY DRAPE PACK |
DYNJ64354A | ENSEMBLE CORONAROGRAPHIE-LF |
0M-CP01029D | RADIOL ANGIO PACK-LF |
DYNJ81454B | ARTERIOGRAM PACK 2 |
DYNJ51338C | CATH PACK |
DYNDH1228 | BRISTOL MYELOGRAM |
DYNJ83961A | CARDIAC CATH-LEFT HEART |
HCP075G | ANGIOGRAPHY DRAPE PACK |
DYNJ85070 | CATH LAB PACK |
DYNJ39515A | CT SCAN PACK |
00-398650AJ | ANGIOGRAPHY DRAPE PACK |
DYNJ24812D | I.R. RADIOLOGY PACK |
DYNJ69974 | (CH) ARTERIOGRAM ADD ON PACK |
DYNJ69135A | BASE HEMODYNAMIE-LF |
DYNJ45020 | INTERVENTIONAL RADIOLOGY PACK |
DYNJ51240A | PORTACATH PACK |
DYNJ43969 | RADIOLOGY PACK |
DYNJ41932I | LEFT HEART SMGH-LF 2 |
0M-CP01029D | RADIOL ANGIO PACK-LF |
DYNJ81454B | ARTERIOGRAM PACK 2 |
- Lot codes and dates
20 of 20 products
Products covered by this recall # Barcodes Product as published 1 1019532715631240195327156313Lot Number: 24IBS428; 2) DYNJ64354A, UDI-DI: 10195327156312(each), 40195327156313(case) 2 1088827785811440888277858115Lot Number: 24JBM450; 3) 0M-CP01029D, UDI-DI: 10888277858114(each), 40888277858115(case) 3 1019845910010940198459100100Lot Number: 24JBM593; 4) DYNJ81454B, UDI-DI: 10198459100109(each), 40198459100100(case) 4 1019348924171640193489241717Lot Number: 24JBN316; 5) DYNJ51338C, UDI-DI: 10193489241716(each), 40193489241717(case) 5 1088994257200740889942572008Lot Number: 24JBN784; 6) DYNDH1228, UDI-DI: 10889942572007(each), 40889942572008(case) 6 1019532751774840195327517749Lot Number: 24JBU509; 7) DYNJ83961A, UDI-DI: 10195327517748(each), 40195327517749(case) 7 1019845913445640198459134457Lot Number: 24JBW818; 8) HCP075G, UDI-DI: 10198459134456(each), 40198459134457(case) 8 1019532745539240195327455393Lot Number: 24JBX138; 9) DYNJ85070, UDI-DI: 10195327455392(each), 40195327455393(case) 9 1088994275313040889942753131Lot Number: 24JBY293; 10) DYNJ39515A, UDI-DI: 10889942753130(each), 40889942753131(case) 10 1019532733090340195327330904Lot Number: 24KBA200; 11) 00-398650AJ, UDI-DI: 10195327330903(each), 40195327330904(case) 11 1088438965321040884389653211Lot Number: 24KBA758; 12) DYNJ24812D, UDI-DI: 10884389653210(each), 40884389653211(case) 12 1019532700111740195327001118Lot Number: 24KBB397; 13) DYNJ69974, UDI-DI: 10195327001117(each), 40195327001118(case) 13 1019532714049640195327140497Lot Number: 24KBB454; 14) DYNJ69135A, UDI-DI: 10195327140496(each), 40195327140497(case) 14 1088827708668540888277086686Lot Number: 24KBC186; 15) DYNJ45020, UDI-DI: 10888277086685(each), 40888277086686(case) 15 1088994249352440889942493525Lot Number: 24KBC962; 16) DYNJ51240A, UDI-DI: 10889942493524(each), 40889942493525(case) 16 1088827707708940888277077080Lot Number: 24KBE652; 17) DYNJ43969, UDI-DI: 10888277077089(each), 40888277077080(case) 17 1019845907869940198459078690Lot Number: 24KBF965; 18) DYNJ41932I, UDI-DI: 10198459078699(each), 40198459078690(case) 18 1088827785811440888277858115Lot Number: 24KBG499; 19) 0M-CP01029D, UDI-DI: 10888277858114(each), 40888277858115(case) 19 1019845910010940198459100100Lot Number: 24KBG961; 20) DYNJ81454B, UDI-DI: 10198459100109(each), 40198459100100(case) 20 Lot 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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