Reported Feb 25, 2026 · Ongoing

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

36 of 36 products

Products covered by this recall
Model / numberProduct as published
CDS820080NC-SECTION PACK
CDS983523GC-SECTION CDS
CDSCCR611OC-SECTION
CDSCCR611PC-SECTION
DYNJ0101616ILUD C-SECTION-LF
DYNJ15494GC-SECTION TRAY
DYNJ19529PC-SECTION TRAY-LF
DYNJ19529QC-SECTION TRAY-LF
DYNJ19529RC-SECTION TRAY-LF
DYNJ19529SC-SECTION TRAY-LF
DYNJ21550QC-SECTION PACK-LF
DYNJ23544FC-SECTION PACK
DYNJ32632FC-SECTION PACK
DYNJ35100IC-SECTION PACK QVH-LF
DYNJ38801FC-SECTION PACK-LF
DYNJ40129CSCRIPPS SW C-SECTION PACK-LF
DYNJ41444FC-SECTION
DYNJ49224IC-SECTION PACK
DYNJ52387IC SECTION PACK-LF
DYNJ56523CC-SECTION PACK
Lot codes and dates

75 of 75 products

Products covered by this recall
#BarcodesProduct as published
11019532728368140195327283682Lot Number: 23IMB818; 2) CDS983523G, UDI-DI: 10195327283681(each), 40195327283682(case)
21019348936790440193489367905Lot Number: 23IBS984; 3) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case)
31019348936790440193489367905Lot Number: 21WBA953; 4) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case)
41019348936790440193489367905Lot Number: 21LBC555; 5) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case)
51019532706585040195327065851Lot Number: 21CBN328; 6) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
61019532706585040195327065851Lot Number: 22IBG757; 7) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
71019532706585040195327065851Lot Number: 22FBU298; 8) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
81019532706585040195327065851Lot Number: 22FBU297; 9) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
91019532706585040195327065851Lot Number: 22FBU296; 10) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
101019532706585040195327065851Lot Number: 22EBA155; 11) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
111019532706585040195327065851Lot Number: 22BBT090; 12) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case)
121019348924881440193489248815Lot Number: 22BBH774; 13) DYNJ0101616I, UDI-DI: 10193489248814(each), 40193489248815(case)
131019348996119540193489961196Lot Number: 21ADA105; 14) DYNJ15494G, UDI-DI: 10193489961195(each), 40193489961196(case)
141019532752933840195327529339Lot Number: 22LBS122; 15) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case)
151019532752933840195327529339Lot Number: 24GMF054; 16) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case)
161019532752933840195327529339Lot Number: 24FMB372; 17) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case)
171019532752933840195327529339Lot Number: 24EMB123; 18) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case)
181019532752933840195327529339Lot Number: 24AMD085; 19) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case)
191019845910936240198459109363Lot Number: 23LME909; 20) DYNJ19529Q, UDI-DI: 10198459109362(each), 40198459109363(case)
201019845910936240198459109363Lot Number: 25BMB041; 21) DYNJ19529Q, UDI-DI: 10198459109362(each), 40198459109363(case)
Amount recalled
4525 units

This recall covers 43 products

The agency filed one notice per product. You are reading one of them; the other 42 are below.

30 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

This product could cause temporary or reversible health problems — stop using it.

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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, 6:58 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.