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?

76 of 76 products

Products covered by this recall
Model / numberBarcodesProduct as published
CDS983639K1019532735153340195327351534UDI/DI 10195327351533 (each), 40195327351534 (case), Lot Number 23FBP157
CDS983639K1019532735153340195327351534UDI/DI 10195327351533 (each), 40195327351534 (case), Lot Number 23GBM569
CDS984267J1019348928887240193489288873UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 23LBN523
CDS984267J1019348928887240193489288873UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24BBA266
CDS984267J1019348928887240193489288873UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24CBS676
CDS984267J1019348928887240193489288873UDI/DI 10193489288872 (each), 40193489288873 (case), Lot Number 24EBM454
DYNJ00264M1019532741871740195327418718UDI/DI 10195327418717 (each), 40195327418718 (case), Lot Number 23HMA639
DYNJ00264M1019532741871740195327418718UDI/DI 10195327418717 (each), 40195327418718 (case), Lot Number 23HMF507
DYNJ0428947L1019532732913640195327329137UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23GMI327
DYNJ0428947L1019532732913640195327329137UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23JMC006
DYNJ0428947L1019532732913640195327329137UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23LMA065
DYNJ0428947L1019532732913640195327329137UDI/DI 10195327329136 (each), 40195327329137 (case), Lot Number 23LMC367
DYNJ0428947M1019532758668340195327586684UDI/DI 10195327586683 (each), 40195327586684 (case), Lot Number 24DMF699
DYNJ0428947M1019532758668340195327586684UDI/DI 10195327586683 (each), 40195327586684 (case), Lot Number 24EMA236
DYNJ27319V1019532720812740195327208128UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23GBI654
DYNJ27319V1019532720812740195327208128UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23GBJ925
DYNJ27319V1019532720812740195327208128UDI/DI 10195327208127 (each), 40195327208128 (case), Lot Number 23HBZ090
DYNJ33977M1019532742252340195327422524UDI/DI 10195327422523 (each), 40195327422524 (case), Lot Number 23HBB046
DYNJ44852M1019532732522040195327325221UDI/DI 10195327325220 (each), 40195327325221 (case), Lot Number 23HME689
DYNJ57527C1019532724347040195327243471UDI/DI 10195327243470 (each), 40195327243471 (case), Lot Number 23GBA730
Amount recalled
4214 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:53 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.