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
#BarcodesProduct as published
11019348985614940193489856140Lot Number: 24IBE926; 2) DYNJ45711B, UDI-DI: 10193489856149(each), 40193489856140(case)
21019348985241740193489852418Lot Number: 24IBE981; 3) DYNJ45266B, UDI-DI: 10193489852417(each), 40193489852418(case)
31019845905085540198459050856Lot Number: 24IBF031; 4) DYNJ80737B, UDI-DI: 10198459050855(each), 40198459050856(case)
41019348994563840193489945639Lot Number: 24IBF165; 5) DYNJ67785A, UDI-DI: 10193489945638(each), 40193489945639(case)
51019845911352940198459113520Lot Number: 24IBG441; 6) DYNJ49675F, UDI-DI: 10198459113529(each), 40198459113520(case)
61088994242984440889942429845Lot Number: 24IBG617; 7) DYNJ0579176B, UDI-DI: 10889942429844(each), 40889942429845(case)
71019348958701240193489587013Lot Number: 24IBG732; 8) DYNJ23615D, UDI-DI: 10193489587012(each), 40193489587013(case)
81019532732234240195327322343Lot Number: 24IBG752; 9) DYNJ44752D, UDI-DI: 10195327322342(each), 40195327322343(case)
91019532723685440195327236855Lot Number: 24IBG844; 10) DYNJ83155, UDI-DI: 10195327236854(each), 40195327236855(case)
101019532726541040195327265411Lot Number: 24IBH261; 11) DYNJ83423, UDI-DI: 10195327265410(each), 40195327265411(case)
111019532744944540195327449446Lot Number: 24IBH595; 12) DYNJ64257C, UDI-DI: 10195327449445(each), 40195327449446(case)
121019845907886640198459078867Lot Number: 24IBH738; 13) DYNJ30587I, UDI-DI: 10198459078866(each), 40198459078867(case)
131019845902747540198459027476Lot Number: 24IBM219; 14) DYNJ58655B, UDI-DI: 10198459027475(each), 40198459027476(case)
141019532763117840195327631179Lot Number: 24IBQ285; 15) DYNJ49308F, UDI-DI: 10195327631178(each), 40195327631179(case)
151088994255931240889942559313Lot Number: 24IBQ350; 16) DYNJ46736B, UDI-DI: 10889942559312(each), 40889942559313(case)
161019845909361640198459093617Lot Number: 24IBQ975; 17) DYNJ27547B, UDI-DI: 10198459093616(each), 40198459093617(case)
171019532746480640195327464807Lot Number: 24IBR473; 18) DYNJ14143J, UDI-DI: 10195327464806(each), 40195327464807(case)
181019532742898340195327428984Lot Number: 24IBR483; 19) DYNJ80819B, UDI-DI: 10195327428983(each), 40195327428984(case)
191088827781687940888277816870Lot Number: 24IBR559; 20) DYNJ47687A, UDI-DI: 10888277816879(each), 40888277816870(case)
201019845903164940198459031640Lot 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.

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, 5:40 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.