Reported May 13, 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
55 of 55 products
| Model / number | Product as published |
|---|---|
CDS820080N | C-SECTION PACK |
CDS983523G | C-SECTION CDS |
CDSCCR611O | C-SECTION |
CDSCCR611P | C-SECTION |
DYNJ0101616I | LUD C-SECTION-LF |
DYNJ15494G | C-SECTION TRAY |
DYNJ19529O | C-SECTION TRAY-LF |
DYNJ19529P | C-SECTION TRAY-LF |
DYNJ19529Q | C-SECTION TRAY-LF |
DYNJ19529R | C-SECTION TRAY-LF |
DYNJ19529S | C-SECTION TRAY-LF |
DYNJ21550Q | C-SECTION PACK-LF |
DYNJ23544F | C-SECTION PACK |
DYNJ32632F | C-SECTION PACK |
DYNJ35100I | C-SECTION PACK QVH-LF |
DYNJ35902F | C-SECTION PACK |
DYNJ38801F | C-SECTION PACK-LF |
DYNJ40129C | SCRIPPS SW C-SECTION PACK-LF |
DYNJ41444F | C-SECTION |
DYNJ49224I | C-SECTION PACK |
- Lot codes and dates
158 of 158 products
Products covered by this recall # Barcodes Product as published 1 1019532728368140195327283682Lot Number: 23IMB818; 2) CDS983523G, UDI-DI: 10195327283681(each), 40195327283682(case) 2 1019348936790440193489367905Lot Number: 23IBS984; 3) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case) 3 1019348936790440193489367905Lot Number: 21CBN328; 4) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case) 4 1019348936790440193489367905Lot Number: 21LBC555; 5) CDSCCR611O, UDI-DI: 10193489367904(each), 40193489367905(case) 5 1019532706585040195327065851Lot Number: 21WBA953; 6) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 6 1019532706585040195327065851Lot Number: 22BBH774; 7) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 7 1019532706585040195327065851Lot Number: 22BBT090; 8) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 8 1019532706585040195327065851Lot Number: 22EBA155; 9) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 9 1019532706585040195327065851Lot Number: 22FBU296; 10) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 10 1019532706585040195327065851Lot Number: 22FBU297; 11) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 11 1019532706585040195327065851Lot Number: 22FBU298; 12) CDSCCR611P, UDI-DI: 10195327065850(each), 40195327065851(case) 12 1019348924881440193489248815Lot Number: 22IBG757; 13) DYNJ0101616I, UDI-DI: 10193489248814(each), 40193489248815(case) 13 1019348996119540193489961196Lot Number: 21ADA105; 14) DYNJ15494G, UDI-DI: 10193489961195(each), 40193489961196(case) 14 1019532729720640195327297207Lot Number: 22LBS122; 15) DYNJ19529O, UDI-DI: 10195327297206(each), 40195327297207(case) 15 1019532729720640195327297207Lot Number: 23CMB465; 16) DYNJ19529O, UDI-DI: 10195327297206(each), 40195327297207(case) 16 1019532729720640195327297207Lot Number: 23DMH505; 17) DYNJ19529O, UDI-DI: 10195327297206(each), 40195327297207(case) 17 1019532729720640195327297207Lot Number: 23FMF781; 18) DYNJ19529O, UDI-DI: 10195327297206(each), 40195327297207(case) 18 1019532729720640195327297207Lot Number: 23IMB944; 19) DYNJ19529O, UDI-DI: 10195327297206(each), 40195327297207(case) 19 1019532752933840195327529339Lot Number: 23IME367; 20) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case) 20 1019532752933840195327529339Lot Number: 23JMD920; 21) DYNJ19529P, UDI-DI: 10195327529338(each), 40195327529339(case) - Amount recalled
- 12529 units
This recall covers 42 products
The agency filed one notice per product. You are reading one of them; the other 41 are below.
29 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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