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

55 of 55 products

Products covered by this recall
Model / numberProduct as published
DYNJ26971LLABOR AND DELIVERY PACK-LF
DYNJ0378319PVAGINAL DELIVERY PACK-LF
DYNJ64017BVUWC OB PACK
DYNJHTLD04AOB PROTECTION PACK NO GAUZE
HM190APACK VAGINAL DELIVERY
SYNJ10248BVAGINAL DELIVERY PACK
DYNJ84209OB PROTECTION PACK NO GAUZE
DYNJ49542BVAG DELIVERY PACK-6220
DYNJ37124CFHT VAG DELIVERY PACK
DYNJ65689VAGINAL DEL PK
DYNJ43737DPK,L&D-VAG DEL
DYNJ0731657ML&D PACK-LF
DYNJ43604BVAGINAL DELIVERY PACK-LF
DYNJ24276CVAD ACCESS
DYNJ80304VAGINAL DELIVERY PACK
CDS982762IVAGINAL DELIVERY CDS
DYNJ903796CVAGINAL DELIVERY
DYNJ43677DVAGINAL DELIVERY PACK
DYNJ43677DVAGINAL DELIVERY PACK
DYNJ47625BBR L&D PACK
Lot codes and dates

55 of 55 products

Products covered by this recall
#BarcodesProduct as published
11019845910572240198459105723Lot Number: 24IBD872; 2) DYNJ0378319P, UDI-DI: 10198459105722(each), 40198459105723(case)
21019532755032540195327550326Lot Number: 24IBF374; 3) DYNJ64017B, UDI-DI: 10195327550325(each), 40195327550326(case)
31019348930334640193489303347Lot Number: 24IBG070; 4) DYNJHTLD04A, UDI-DI: 10193489303346(each), 40193489303347(case)
41019532730516140195327305162Lot Number: 24IBH288; 5) HM190A, UDI-DI: 10195327305161(each), 40195327305162(case)
51019348937338740193489373388Lot Number: 24IBH818; 6) SYNJ10248B, UDI-DI: 10193489373387(each), 40193489373388(case)
61019532734273940195327342730Lot Number: 24IBH820; 7) DYNJ84209, UDI-DI: 10195327342739(each), 40195327342730(case)
71019532738807240195327388073Lot Number: 24IBH988; 8) DYNJ49542B, UDI-DI: 10195327388072(each), 40195327388073(case)
81019532741619540195327416196Lot Number: 24IBR452; 9) DYNJ37124C, UDI-DI: 10195327416195(each), 40195327416196(case)
91019348928483640193489284837Lot Number: 24IBR491; 10) DYNJ65689, UDI-DI: 10193489284836(each), 40193489284837(case)
101019348935084540193489350846Lot Number: 24IBR570; 11) DYNJ43737D, UDI-DI: 10193489350845(each), 40193489350846(case)
111019532769702040195327697021Lot Number: 24IBR650; 12) DYNJ0731657M, UDI-DI: 10195327697020(each), 40195327697021(case)
121019348999752140193489997522Lot Number: 24IBR661; 13) DYNJ43604B, UDI-DI: 10193489997521(each), 40193489997522(case)
131088438943118440884389431185Lot Number: 24IBR707; 14) DYNJ24276C, UDI-DI: 10884389431184(each), 40884389431185(case)
141019532702253240195327022533Lot Number: 24IBS408; 15) DYNJ80304, UDI-DI: 10195327022532(each), 40195327022533(case)
151019348994209540193489942096Lot Number: 24IBS686; 16) CDS982762I, UDI-DI: 10193489942095(each), 40193489942096(case)
161019532762337140195327623372Lot Number: 24JBB609; 17) DYNJ903796C, UDI-DI: 10195327623371(each), 40195327623372(case)
171019348976858940193489768580Lot Number: 24JBE762; 18) DYNJ43677D, UDI-DI: 10193489768589(each), 40193489768580(case)
181019348976858940193489768580Lot Number: 24JBM324; 19) DYNJ43677D, UDI-DI: 10193489768589(each), 40193489768580(case)
191088994218258940889942182580Lot Number: 24JBM600; 20) DYNJ47625B, UDI-DI: 10889942182589(each), 40889942182580(case)
201019532719109240195327191093Lot Number: 24JBN320; 21) DYNJ03387B, UDI-DI: 10195327191092(each), 40195327191093(case)
Amount recalled
21935 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, 6:59 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.