Reported Nov 26, 2025 · Ongoing
MEDLINE convenience kits labeled as
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 labeled as
67 of 67 products
| Model / number | Product as published |
|---|---|
CDS930027W | GENERAL LAPAROSCOPY |
CDS980245X | GENERAL MAJOR CDS |
CDS980566F | BASIC GENERAL CDS |
CDS982823R | TOTAL KNEE CDS |
CDS982936U | BASIC CDS |
CDS983907M | UPPER EXTREMITY CDS |
CDS983908Q | MAJOR ABDOMINAL CDS |
CDS983909Q | LOWER EXTREMITY CDS |
CDS983914M | GENERAL SURGERY CDS |
CDS983915N | GENERAL ORTHO CDS |
CDS984251O | GENERAL LAP |
CDS984262O | ROBOTIC |
DYNJ00282Q | HYPOSPADIUS PACK |
DYNJ0161694F | MINOR HARPER PACK-LF |
DYNJ0161832F | THROMBECTOMY HARPER PACK-LF |
DYNJ0161949C | MAJOR COMPONENT HARPER PACK-LF |
DYNJ0259893T | MINOR PACK-LF |
DYNJ0368519AA | TOTAL KNEE PACK LF |
DYNJ0368519Y | TOTAL KNEE PACK LF |
DYNJ0406353N | PEDIATRIC BASIC PACK-LF |
- Lot codes and dates
220 of 220 products
Products covered by this recall Model / number Barcodes Product as published 24BBC8601019532760149240195327601493UDI/DI 10195327601492 (each), 40195327601493 (case), Lot Numbers: 24BBC860 24BBU6071019348984843440193489848435UDI/DI 10193489848434 (each), 40193489848435 (case), Lot Numbers: 24BBU607 24CBU5831019348984843440193489848435UDI/DI 10193489848434 (each), 40193489848435 (case), Lot Numbers: 24CBU583 24EBE5461019348984843440193489848435UDI/DI 10193489848434 (each), 40193489848435 (case), Lot Numbers: 24EBE546 23GBF7331019348944544240193489445443UDI/DI 10193489445442 (each), 40193489445443 (case), Lot Numbers: 23GBF733 24ABG1401019348944544240193489445443UDI/DI 10193489445442 (each), 40193489445443 (case), Lot Numbers: 24ABG140 24BBN5211019348944544240193489445443UDI/DI 10193489445442 (each), 40193489445443 (case), Lot Numbers: 24BBN521 24CBR6961019348944544240193489445443UDI/DI 10193489445442 (each), 40193489445443 (case), Lot Numbers: 24CBR696 24EBK8571019348944544240193489445443UDI/DI 10193489445442 (each), 40193489445443 (case), Lot Numbers: 24EBK857 24ABH2001019532758448140195327584482UDI/DI 10195327584481 (each), 40195327584482 (case), Lot Numbers: 24ABH200 24BBG7871019532758448140195327584482UDI/DI 10195327584481 (each), 40195327584482 (case), Lot Numbers: 24BBG787 24CBI6791019532758448140195327584482UDI/DI 10195327584481 (each), 40195327584482 (case), Lot Numbers: 24CBI679 23GBS7001019532718522040195327185221UDI/DI 10195327185220 (each), 40195327185221 (case), Lot Numbers: 23GBS700 24ABG3631019532718522040195327185221UDI/DI 10195327185220 (each), 40195327185221 (case), Lot Numbers: 24ABG363 24BBH9501019532758449840195327584499UDI/DI 10195327584498 (each), 40195327584499 (case), Lot Numbers: 24BBH950 24BBR4201019532758449840195327584499UDI/DI 10195327584498 (each), 40195327584499 (case), Lot Numbers: 24BBR420 24CBV4741019532758449840195327584499UDI/DI 10195327584498 (each), 40195327584499 (case), Lot Numbers: 24CBV474 24EBS6191019532758449840195327584499UDI/DI 10195327584498 (each), 40195327584499 (case), Lot Numbers: 24EBS619 24ABQ7671019532758445040195327584451UDI/DI 10195327584450 (each), 40195327584451 (case), Lot Numbers: 24ABQ767 24ABS3331019532758445040195327584451UDI/DI 10195327584450 (each), 40195327584451 (case), Lot Numbers: 24ABS333 - Amount recalled
- 20941 kits
This recall covers 21 products
The agency filed one notice per product. You are reading one of them; the other 20 are below.
8 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing SafeAir Smoke Evacuation Pencils. Stryker Instruments has expanded the scope of their recall of SafeAir Smoke Evacuation Pencils previously initiated in October 2024, adding an additional 47 lots to the scope of the recall. The initial recall was due to the potential for product to activate without manual input when plugged into a power source or remain active after buttons are released.
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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