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

170 of 170 products

Products covered by this recall
#BarcodesProduct as published
11088994285112640889942851127Lot Number: 24IBE784; 2) DYNJ50017B, UDI-DI: 10889942851126(each), 40889942851127(case)
21019845909156840198459091569Lot Number: 24IBE809; 3) DYNJ68242C, UDI-DI: 10198459091568(each), 40198459091569(case)
31019532706797740195327067978Lot Number: 24IBF050; 4) SYNJ10001B, UDI-DI: 10195327067977(each), 40195327067978(case)
41088827700350740888277003508Lot Number: 24IBF241; 5) DYNJ42691, UDI-DI: 10888277003507(each), 40888277003508(case)
51088994276319140889942763192Lot Number: 24IBF320; 6) DYNJ43775C, UDI-DI: 10889942763191(each), 40889942763192(case)
61019348952863340193489528634Lot Number: 24IBF620; 7) DYNJ54078A, UDI-DI: 10193489528633(each), 40193489528634(case)
71088994266999840889942669999Lot Number: 24IBF640; 8) DYNJ39493B, UDI-DI: 10889942669998(each), 40889942669999(case)
81019532766166340195327661664Lot Number: 24IBG032; 9) DYNJ0101397O, UDI-DI: 10195327661663(each), 40195327661664(case)
91019532727968440195327279685Lot Number: 24IBG201; 10) DYNJ28408J, UDI-DI: 10195327279684(each), 40195327279685(case)
101088994268436640889942684367Lot Number: 24IBG536; 11) DYNJ45997C, UDI-DI: 10889942684366(each), 40889942684367(case)
111019532722447940195327224470Lot Number: 24IBG574; 12) DYNJ17504G, UDI-DI: 10195327224479(each), 40195327224470(case)
121019532746370040195327463701Lot Number: 24IBG595; 13) DYNJ44532D, UDI-DI: 10195327463700(each), 40195327463701(case)
131019532762169840195327621699Lot Number: 24IBG706; 14) DYNJ65996C, UDI-DI: 10195327621698(each), 40195327621699(case)
141019348988346640193489883467Lot Number: 24IBG871; 15) DYNJ63703B, UDI-DI: 10193489883466(each), 40193489883467(case)
151019348968537440193489685375Lot Number: 24IBH017; 16) DYNJ59621A, UDI-DI: 10193489685374(each), 40193489685375(case)
161088994277571240889942775713Lot Number: 24IBH300; 17) DYNJ37733B, UDI-DI: 10889942775712(each), 40889942775713(case)
171019348953289040193489532891Lot Number: 24IBH634; 18) DYKE1321B, UDI-DI: 10193489532890(each), 40193489532891(case)
181088994236161840889942361619Lot Number: 24IBH701; 19) DYNJ24860G, UDI-DI: 10889942361618(each), 40889942361619(case)
191019532713064040195327130641Lot Number: 24IBH843; 20) DYNJ81648, UDI-DI: 10195327130640(each), 40195327130641(case)
201019532738625240195327386253Lot Number: 24IBH845; 21) DYNJ84619, UDI-DI: 10195327386252(each), 40195327386253(case)
Amount recalled
28127 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, 5:32 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.