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

107 of 107 products

Products covered by this recall
#BarcodesProduct as published
11019532760907840195327609079Lot Number: 24IBF062; 2) DYNJ31798D, UDI-DI: 10195327609078(each), 40195327609079(case)
21019348993318540193489933186Lot Number: 24IBF219; 3) DYNJ46311F, UDI-DI: 10193489933185(each), 40193489933186(case)
31088994229288240889942292883Lot Number: 24IBF751; 4) DYNJ49386A, UDI-DI: 10889942292882(each), 40889942292883(case)
41019845904597440198459045975Lot Number: 24IBF768; 5) DYNJ51781G, UDI-DI: 10198459045974(each), 40198459045975(case)
51019532769856040195327698561Lot Number: 24IBG614; 6) DYNJ54474C, UDI-DI: 10195327698560(each), 40195327698561(case)
61019348993318540193489933186Lot Number: 24IBG988; 7) DYNJ46311F, UDI-DI: 10193489933185(each), 40193489933186(case)
71019348926888140193489268882Lot Number: 24IBH023; 8) DYNJ65348, UDI-DI: 10193489268881(each), 40193489268882(case)
81019348996155340193489961554Lot Number: 24IBH081; 9) DYNJ37322I, UDI-DI: 10193489961553(each), 40193489961554(case)
91019532715360140195327153602Lot Number: 24IBH579; 10) DYNJ69926A, UDI-DI: 10195327153601(each), 40195327153602(case)
101088438984207240884389842073Lot Number: 24IBH589; 11) DYNJ39903, UDI-DI: 10884389842072(each), 40884389842073(case)
111019348937025640193489370257Lot Number: 24IBH647; 12) DYNJ47816B, UDI-DI: 10193489370256(each), 40193489370257(case)
121019348937359240193489373593Lot Number: 24IBH806; 13) SYNJ10253B, UDI-DI: 10193489373592(each), 40193489373593(case)
131088994237346840889942373469Lot Number: 24IBH821; 14) DYNJ31169C, UDI-DI: 10889942373468(each), 40889942373469(case)
141088994272564940889942725640Lot Number: 24IBK285; 15) DYNJ06622J, UDI-DI: 10889942725649(each), 40889942725640(case)
151019532726291440195327262915Lot Number: 24IBQ232; 16) DYNJ83390, UDI-DI: 10195327262914(each), 40195327262915(case)
161088438926022740884389260228Lot Number: 24IBQ640; 17) DYNJ33236, UDI-DI: 10884389260227(each), 40884389260228(case)
171019348942974940193489429740Lot Number: 24IBR149; 18) DYNDH1510, UDI-DI: 10193489429749(each), 40193489429740(case)
181019845902211140198459022112Lot Number: 24IBR168; 19) DYNJ52928D, UDI-DI: 10198459022111(each), 40198459022112(case)
191019532724234340195327242344Lot Number: 24IBR186; 20) DYNJ35021D, UDI-DI: 10195327242343(each), 40195327242344(case)
201019348937359240193489373593Lot Number: 24IBR323; 21) SYNJ10253B, UDI-DI: 10193489373592(each), 40193489373593(case)
Amount recalled
11889 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, 4:54 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.