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
| Model / number | Product as published |
|---|---|
MNS13635A | ED CRASH C-SECTION TRAY |
DYNJ81281 | C-SECTION PCH-LF |
OBK387M | C-SECTION PACK-LF |
DYNJ81281 | C-SECTION PCH-LF |
DYNJ40573A | NHS - C-SECTION SCG |
CDS983998C | C-SECTION CDS |
DYNJ64300A | C-SECTION ADD ON PACK |
DYNJ55205 | EMERGENCY BIRTH PACK |
DYNJ56550 | C-SECTION PACK |
DYNJ83507 | C-SECTION ADD ON PACK |
DYNJ83248 | C-SECTION CLOSURE PACK |
DYNJ81281 | C-SECTION PCH-LF |
- Lot codes and dates
12 of 12 products
Products covered by this recall # Barcodes Product as published 1 1019532710362040195327103621Lot Number: 24IBH747; 2) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case) 2 1088994268681040889942686811Lot Number: 24JBM309; 3) OBK387M, UDI-DI: 10889942686810(each), 40889942686811(case) 3 1019532710362040195327103621Lot Number: 24JBM385; 4) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case) 4 1088827798851440888277988515Lot Number: 24JBM576; 5) DYNJ40573A, UDI-DI: 10888277988514(each), 40888277988515(case) 5 1019348977671340193489776714Lot Number: 24JBM871; 6) CDS983998C, UDI-DI: 10193489776713(each), 40193489776714(case) 6 1019348985237040193489852371Lot Number: 24JBS915; 7) DYNJ64300A, UDI-DI: 10193489852370(each), 40193489852371(case) 7 1088994253280340889942532804Lot Number: 24JBU461; 8) DYNJ55205, UDI-DI: 10889942532803(each), 40889942532804(case) 8 1088994267177940889942671770Lot Number: 24JBV449; 9) DYNJ56550, UDI-DI: 10889942671779(each), 40889942671770(case) 9 1019532727307140195327273072Lot Number: 24JBV561; 10) DYNJ83507, UDI-DI: 10195327273071(each), 40195327273072(case) 10 1019532724838340195327248384Lot Number: 24JBX835; 11) DYNJ83248, UDI-DI: 10195327248383(each), 40195327248384(case) 11 1019532710362040195327103621Lot Number: 24KBF051; 12) DYNJ81281, UDI-DI: 10195327103620(each), 40195327103621(case) 12 Lot 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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