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

12 of 12 products

Products covered by this recall
Model / numberProduct as published
MNS13635AED CRASH C-SECTION TRAY
DYNJ81281C-SECTION PCH-LF
OBK387MC-SECTION PACK-LF
DYNJ81281C-SECTION PCH-LF
DYNJ40573ANHS - C-SECTION SCG
CDS983998CC-SECTION CDS
DYNJ64300AC-SECTION ADD ON PACK
DYNJ55205EMERGENCY BIRTH PACK
DYNJ56550C-SECTION PACK
DYNJ83507C-SECTION ADD ON PACK
DYNJ83248C-SECTION CLOSURE PACK
DYNJ81281C-SECTION PCH-LF
Lot codes and dates

12 of 12 products

Products covered by this recall
#BarcodesProduct as published
11019532710362040195327103621Lot Number: 24IBH747; 2) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case)
21088994268681040889942686811Lot Number: 24JBM309; 3) OBK387M, UDI-DI: 10889942686810(each), 40889942686811(case)
31019532710362040195327103621Lot Number: 24JBM385; 4) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case)
41088827798851440888277988515Lot Number: 24JBM576; 5) DYNJ40573A, UDI-DI: 10888277988514(each), 40888277988515(case)
51019348977671340193489776714Lot Number: 24JBM871; 6) CDS983998C, UDI-DI: 10193489776713(each), 40193489776714(case)
61019348985237040193489852371Lot Number: 24JBS915; 7) DYNJ64300A, UDI-DI: 10193489852370(each), 40193489852371(case)
71088994253280340889942532804Lot Number: 24JBU461; 8) DYNJ55205, UDI-DI: 10889942532803(each), 40889942532804(case)
81088994267177940889942671770Lot Number: 24JBV449; 9) DYNJ56550, UDI-DI: 10889942671779(each), 40889942671770(case)
91019532727307140195327273072Lot Number: 24JBV561; 10) DYNJ83507, UDI-DI: 10195327273071(each), 40195327273072(case)
101019532724838340195327248384Lot Number: 24JBX835; 11) DYNJ83248, UDI-DI: 10195327248383(each), 40195327248384(case)
111019532710362040195327103621Lot Number: 24KBF051; 12) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case)
12Lot Number: 24KBG874
Amount recalled
1098 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, 5:41 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.