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
24 of 24 products
| Model / number | Product as published |
|---|---|
DYNJ68673 | UTHET TYLER OB PACK |
DYNJ66290A | D AND C PACK |
DYNJ24159C | D & C PACK-LF |
DYNJ54484A | OB PACK |
DYNJS3040 | PERI GYN-LF |
DYNJ900422F | D&C |
CDS985201A | D&C HYSTEROSCOPY CDS |
DYNJ66290A | D AND C PACK |
DYNJ47616B | D&C PACK |
DYNJ50656B | WMC D & C PACK-LF |
DYNJ36599 | TRANSVAGINAL PACK |
DYNJ25915G | OB PACK |
DYNJS3040 | PERI GYN-LF |
DYNJ0989660A | MEMORIAL D AND C PACK |
DYNJ64226A | HYSTEROSCOPY PACK |
DYNJ64571 | OB PACK |
DYNJ50656B | WMC D & C PACK-LF |
DYNJT2535G | D & C PACK-LF |
DYNJ44522B | OB PACK |
DYNJ26121G | OB PACK-LF |
- Lot codes and dates
24 of 24 products
Products covered by this recall # Barcodes Product as published 1 1019348946142840193489461429Lot Number: 24IBG873; 2) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case) 2 1019845903239440198459032395Lot Number: 24IBG957; 3) DYNJ24159C, UDI-DI: 10198459032394(each), 40198459032395(case) 3 1019348981307440193489813075Lot Number: 24IBL229; 4) DYNJ54484A, UDI-DI: 10193489813074(each), 40193489813075(case) 4 1088438960222540884389602226Lot Number: 24IBS805; 5) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case) 5 1019532765837340195327658374Lot Number: 24JBL655; 6) DYNJ900422F, UDI-DI: 10195327658373(each), 40195327658374(case) 6 1088994294231240889942942313Lot Number: 24JBM234; 7) CDS985201A, UDI-DI: 10889942942312(each), 40889942942313(case) 7 1019348946142840193489461429Lot Number: 24JBN479; 8) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case) 8 1019348973104040193489731041Lot Number: 24JBN645; 9) DYNJ47616B, UDI-DI: 10193489731040(each), 40193489731041(case) 9 1019532730641040195327306411Lot Number: 24JBT461; 10) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case) 10 1088438955414240884389554143Lot Number: 24JBT906; 11) DYNJ36599, UDI-DI: 10884389554142(each), 40884389554143(case) 11 1019348971894240193489718943Lot Number: 24JBW173; 12) DYNJ25915G, UDI-DI: 10193489718942(each), 40193489718943(case) 12 1088438960222540884389602226Lot Number: 24JBW203; 13) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case) 13 1088994213613140889942136132Lot Number: 24JBW545; 14) DYNJ0989660A, UDI-DI: 10889942136131(each), 40889942136132(case) 14 1019532713543040195327135431Lot Number: 24JBX677; 15) DYNJ64226A, UDI-DI: 10195327135430(each), 40195327135431(case) 15 1019348920898640193489208987Lot Number: 24KBC728; 16) DYNJ64571, UDI-DI: 10193489208986(each), 40193489208987(case) 16 1019532730641040195327306411Lot Number: 24KBD692; 17) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case) 17 1019532754850640195327548507Lot Number: 24KBF096; 18) DYNJT2535G, UDI-DI: 10195327548506(each), 40195327548507(case) 18 1019348969151140193489691512Lot Number: 24KBG398; 19) DYNJ44522B, UDI-DI: 10193489691511(each), 40193489691512(case) 19 1088994222524840889942225249Lot Number: 24KBG967; 20) DYNJ26121G, UDI-DI: 10889942225248(each), 40889942225249(case) 20 1019348924724440193489247245Lot Number: 24KBG978; 21) DYNJ905534C, UDI-DI: 10193489247244(each), 40193489247245(case) - Amount recalled
- 2,531 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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