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

Products covered by this recall
Model / numberProduct as published
DYNJ68673UTHET TYLER OB PACK
DYNJ66290AD AND C PACK
DYNJ24159CD & C PACK-LF
DYNJ54484AOB PACK
DYNJS3040PERI GYN-LF
DYNJ900422FD&C
CDS985201AD&C HYSTEROSCOPY CDS
DYNJ66290AD AND C PACK
DYNJ47616BD&C PACK
DYNJ50656BWMC D & C PACK-LF
DYNJ36599TRANSVAGINAL PACK
DYNJ25915GOB PACK
DYNJS3040PERI GYN-LF
DYNJ0989660AMEMORIAL D AND C PACK
DYNJ64226AHYSTEROSCOPY PACK
DYNJ64571OB PACK
DYNJ50656BWMC D & C PACK-LF
DYNJT2535GD & C PACK-LF
DYNJ44522BOB PACK
DYNJ26121GOB PACK-LF
Lot codes and dates

24 of 24 products

Products covered by this recall
#BarcodesProduct as published
11019348946142840193489461429Lot Number: 24IBG873; 2) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case)
21019845903239440198459032395Lot Number: 24IBG957; 3) DYNJ24159C, UDI-DI: 10198459032394(each), 40198459032395(case)
31019348981307440193489813075Lot Number: 24IBL229; 4) DYNJ54484A, UDI-DI: 10193489813074(each), 40193489813075(case)
41088438960222540884389602226Lot Number: 24IBS805; 5) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case)
51019532765837340195327658374Lot Number: 24JBL655; 6) DYNJ900422F, UDI-DI: 10195327658373(each), 40195327658374(case)
61088994294231240889942942313Lot Number: 24JBM234; 7) CDS985201A, UDI-DI: 10889942942312(each), 40889942942313(case)
71019348946142840193489461429Lot Number: 24JBN479; 8) DYNJ66290A, UDI-DI: 10193489461428(each), 40193489461429(case)
81019348973104040193489731041Lot Number: 24JBN645; 9) DYNJ47616B, UDI-DI: 10193489731040(each), 40193489731041(case)
91019532730641040195327306411Lot Number: 24JBT461; 10) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case)
101088438955414240884389554143Lot Number: 24JBT906; 11) DYNJ36599, UDI-DI: 10884389554142(each), 40884389554143(case)
111019348971894240193489718943Lot Number: 24JBW173; 12) DYNJ25915G, UDI-DI: 10193489718942(each), 40193489718943(case)
121088438960222540884389602226Lot Number: 24JBW203; 13) DYNJS3040, UDI-DI: 10884389602225(each), 40884389602226(case)
131088994213613140889942136132Lot Number: 24JBW545; 14) DYNJ0989660A, UDI-DI: 10889942136131(each), 40889942136132(case)
141019532713543040195327135431Lot Number: 24JBX677; 15) DYNJ64226A, UDI-DI: 10195327135430(each), 40195327135431(case)
151019348920898640193489208987Lot Number: 24KBC728; 16) DYNJ64571, UDI-DI: 10193489208986(each), 40193489208987(case)
161019532730641040195327306411Lot Number: 24KBD692; 17) DYNJ50656B, UDI-DI: 10195327306410(each), 40195327306411(case)
171019532754850640195327548507Lot Number: 24KBF096; 18) DYNJT2535G, UDI-DI: 10195327548506(each), 40195327548507(case)
181019348969151140193489691512Lot Number: 24KBG398; 19) DYNJ44522B, UDI-DI: 10193489691511(each), 40193489691512(case)
191088994222524840889942225249Lot Number: 24KBG967; 20) DYNJ26121G, UDI-DI: 10889942225248(each), 40889942225249(case)
201019348924724440193489247245Lot 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:37 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.