Reported Sep 30, 2026 · Ongoing · Updated Oct 24, 2026

Medline Convenience Kits

Medline Industries, LP

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 · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Convenience Kits

28 of 28 products

Products covered by this recall
Model / numberProduct as published
DYNJT10197ANTERIOR SPINE PACK
DYNJVB91001CRANIOTOMY #IMF 56646-LF
DYNJ0369348OCRANIOTOMY PACK-LF
DYNJ0369348PSLUH CRANIOTOMY PACK-LF
DYNJ04342MLAMINECTOMY PACK-LF
DYNJ43218GLAMINECTOMY PACK-LF
DYNJ46024FCRANIOTOMY PACK
DYNJ46070CLAMINECTOMY PACK-LF
DYNJ46672BCRANI PACK
DYNJ52961ISPINE TRAY II
DYNJ53518CSPINE PACK
DYNJ54479CSPINE PACK
DYNJ57815CRANI ADJUNCT PACK
DYNJ57971CWC SPINE PACK-LF
DYNJ59338CPEDI CRANI MAJOR
DYNJ66742CLAMINECTOMY PACK-LF
DYNJ67543BSPINAL PACK-LF
DYNJ69214ALAMINECTOMY PACK
DYNJ83098EPCH LAMINECTOMY I PACK
DYNJ900269ISPINE
Lot codes and dates

109 of 109 products

Products covered by this recall
#BarcodesProduct as published
11019348980117040193489801171Lot Number: 26GBA998; 2) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case)
21019348980117040193489801171Lot Number: 23HLA649; 3) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case)
31019348980117040193489801171Lot Number: 23GLA935; 4) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case)
41019348980117040193489801171Lot Number: 23GLA081; 5) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case)
51019348980117040193489801171Lot Number: 23CLA457; 6) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case)
61019532702589240195327025893Lot Number: 23BLA516; 7) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case)
71019532702589240195327025893Lot Number: 22IBO169; 8) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case)
81019532702589240195327025893Lot Number: 22GBD964; 9) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case)
91019532729541740195327295418Lot Number: 22DBU156; 10) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
101019532729541740195327295418Lot Number: 24KBH955; 11) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
111019532729541740195327295418Lot Number: 24JBB595; 12) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
121019532729541740195327295418Lot Number: 24GMF624; 13) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
131019532729541740195327295418Lot Number: 24CMJ263; 14) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
141019532729541740195327295418Lot Number: 24BMK244; 15) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
151019532729541740195327295418Lot Number: 24AMF230; 16) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
161019532729541740195327295418Lot Number: 23JBJ151; 17) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
171019532729541740195327295418Lot Number: 23FBG216; 18) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
181019532729541740195327295418Lot Number: 23EBC638; 19) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
191019532729541740195327295418Lot Number: 23CBI768; 20) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
201019532729541740195327295418Lot Number: 23ABM980; 21) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case)
Amount recalled
4013 kits

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

  • Nationwide

Why it was recalled

The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.

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 Nov 4, 1:46 AM 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.