Reported Apr 23, 2025 · Ongoing
Refer to RES
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?
- Refer to RES
- Lot codes and dates
121 of 121 products
Products covered by this recall # Barcodes Product as published 1 1019348985614940193489856140Lot Number: 24IBE926; 2) DYNJ45711B, UDI-DI: 10193489856149(each), 40193489856140(case) 2 1019348985241740193489852418Lot Number: 24IBE981; 3) DYNJ45266B, UDI-DI: 10193489852417(each), 40193489852418(case) 3 1019845905085540198459050856Lot Number: 24IBF031; 4) DYNJ80737B, UDI-DI: 10198459050855(each), 40198459050856(case) 4 1019348994563840193489945639Lot Number: 24IBF165; 5) DYNJ67785A, UDI-DI: 10193489945638(each), 40193489945639(case) 5 1019845911352940198459113520Lot Number: 24IBG441; 6) DYNJ49675F, UDI-DI: 10198459113529(each), 40198459113520(case) 6 1088994242984440889942429845Lot Number: 24IBG617; 7) DYNJ0579176B, UDI-DI: 10889942429844(each), 40889942429845(case) 7 1019348958701240193489587013Lot Number: 24IBG732; 8) DYNJ23615D, UDI-DI: 10193489587012(each), 40193489587013(case) 8 1019532732234240195327322343Lot Number: 24IBG752; 9) DYNJ44752D, UDI-DI: 10195327322342(each), 40195327322343(case) 9 1019532723685440195327236855Lot Number: 24IBG844; 10) DYNJ83155, UDI-DI: 10195327236854(each), 40195327236855(case) 10 1019532726541040195327265411Lot Number: 24IBH261; 11) DYNJ83423, UDI-DI: 10195327265410(each), 40195327265411(case) 11 1019532744944540195327449446Lot Number: 24IBH595; 12) DYNJ64257C, UDI-DI: 10195327449445(each), 40195327449446(case) 12 1019845907886640198459078867Lot Number: 24IBH738; 13) DYNJ30587I, UDI-DI: 10198459078866(each), 40198459078867(case) 13 1019845902747540198459027476Lot Number: 24IBM219; 14) DYNJ58655B, UDI-DI: 10198459027475(each), 40198459027476(case) 14 1019532763117840195327631179Lot Number: 24IBQ285; 15) DYNJ49308F, UDI-DI: 10195327631178(each), 40195327631179(case) 15 1088994255931240889942559313Lot Number: 24IBQ350; 16) DYNJ46736B, UDI-DI: 10889942559312(each), 40889942559313(case) 16 1019845909361640198459093617Lot Number: 24IBQ975; 17) DYNJ27547B, UDI-DI: 10198459093616(each), 40198459093617(case) 17 1019532746480640195327464807Lot Number: 24IBR473; 18) DYNJ14143J, UDI-DI: 10195327464806(each), 40195327464807(case) 18 1019532742898340195327428984Lot Number: 24IBR483; 19) DYNJ80819B, UDI-DI: 10195327428983(each), 40195327428984(case) 19 1088827781687940888277816870Lot Number: 24IBR559; 20) DYNJ47687A, UDI-DI: 10888277816879(each), 40888277816870(case) 20 1019845903164940198459031640Lot Number: 24IBR569; 21) DYNJ86034A, UDI-DI: 10198459031649(each), 40198459031640(case) - Amount recalled
- 14760 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.
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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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