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

37 of 37 products

Products covered by this recall
Model / numberProduct as published
DYNJ59310DDR. KHAN CABG ADDS PACK
DYNJ32436ACARDIAC STERNAL PACK
DYNJ35586GVEIN CLOSURE PACK
DYNJ55343BABLATION PACK-LF
DYNJ55343BABLATION PACK-LF
DYNJ65027BCARDIAC PACK
DYNJ48196CVASCULAR PACK-LF
DYNJ40480IMPLANT PACK
DYNJ900523BOPEN HEART
DYNJ19758IPACEMAKER PACK-LF
SYNJ10280CCHOG VP SHUNT PACK
DYNJ48196CVASCULAR PACK-LF
DYNJ27949FEP PACK-LF
DYNJ41874CPACEMAKER PACK WRO-LF
DYNJ83208ACARDIAC PACK OPTION 1
DYNJ56729EP DRAPE PACK
DYNJCD0326CSTM EP PACEMAKER DRAPE PACK
DYNJ80084MINOR INTERVENTIONAL TRAY
DYNJ39111ACT PACK
DYNJ25102IVASCULAR PACK-LF
Lot codes and dates

37 of 37 products

Products covered by this recall
#BarcodesProduct as published
11088438968661440884389686615Lot Number: 24IBB643; 2) DYNJ32436A, UDI-DI: 10884389686614(each), 40884389686615(case)
21019348966323540193489663236Lot Number: 24IBG295; 3) DYNJ35586G, UDI-DI: 10193489663235(each), 40193489663236(case)
31019532747805640195327478057Lot Number: 24IBG343; 4) DYNJ55343B, UDI-DI: 10195327478056(each), 40195327478057(case)
41019532747805640195327478057Lot Number: 24IBG535; 5) DYNJ55343B, UDI-DI: 10195327478056(each), 40195327478057(case)
51019348947199140193489471992Lot Number: 24IBH248; 6) DYNJ65027B, UDI-DI: 10193489471991(each), 40193489471992(case)
61019348971246940193489712460Lot Number: 24IBH653; 7) DYNJ48196C, UDI-DI: 10193489712469(each), 40193489712460(case)
71088438986119640884389861197Lot Number: 24IBL194; 8) DYNJ40480, UDI-DI: 10884389861196(each), 40884389861197(case)
81019532762870340195327628704Lot Number: 24IBO308; 9) DYNJ900523B, UDI-DI: 10195327628703(each), 40195327628704(case)
91019348999232840193489992329Lot Number: 24IBT180; 10) DYNJ19758I, UDI-DI: 10193489992328(each), 40193489992329(case)
101019532737359740195327373598Lot Number: 24IBV182; 11) SYNJ10280C, UDI-DI: 10195327373597(each), 40195327373598(case)
111019348971246940193489712460Lot Number: 24JBL521; 12) DYNJ48196C, UDI-DI: 10193489712469(each), 40193489712460(case)
121019532701610440195327016105Lot Number: 24JBM305; 13) DYNJ27949F, UDI-DI: 10195327016104(each), 40195327016105(case)
131019532742891440195327428915Lot Number: 24JBM849; 14) DYNJ41874C, UDI-DI: 10195327428914(each), 40195327428915(case)
141019845909706540198459097066Lot Number: 24JBM893; 15) DYNJ83208A, UDI-DI: 10198459097065(each), 40198459097066(case)
151088994267602640889942676027Lot Number: 24JBM959; 16) DYNJ56729, UDI-DI: 10889942676026(each), 40889942676027(case)
161019348920350940193489203500Lot Number: 24JBT045; 17) DYNJCD0326, UDI-DI: 10193489203509(each), 40193489203500(case)
171019532701201440195327012015Lot Number: 24JBU078; 18) DYNJ80084, UDI-DI: 10195327012014(each), 40195327012015(case)
181019532742974440195327429745Lot Number: 24JBU113; 19) DYNJ39111A, UDI-DI: 10195327429744(each), 40195327429745(case)
191019532757381240195327573813Lot Number: 24JBU159; 20) DYNJ25102I, UDI-DI: 10195327573812(each), 40195327573813(case)
201019348964692440193489646925Lot Number: 24JBU436; 21) DYNJ62339, UDI-DI: 10193489646924(each), 40193489646925(case)
Amount recalled
3205 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, 5:40 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.