Reported Nov 26, 2025 · Ongoing

MEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3)…

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
    • 1) MINOR SINGLE BASIN PACK
    • REF DYNJ37698L
    • 2) BASIN PACK
    • REF DYNJ50123D
    • 3) MAJOR BASIN PACK
    • REF DYNJ59816A
    • 4) OSC BASIN PACK
    • REF DYNJ68217A
Lot codes and dates

4 of 4 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJ37698L1019532743552340195327435524UDI/DI 10195327435523 (each) 40195327435524, (case), Lot Numbers: 23KMG076, 24AMA944, 24FMA911
DYNJ50123D1019532720199940195327201990UDI/DI 10195327201999 (each) 40195327201990, (case), Lot Numbers: 23FBP789, 24ABG308, 24BBQ467, 24DBP157
DYNJ59816A1019532733157340195327331574UDI/DI 10195327331573 (each) 40195327331574, (case), Lot Numbers: 23GBR142, 23IBJ642, 23LBD170, 23LBM241
DYNJ68217A1019532735252340195327352524UDI/DI 10195327352523 (each) 40195327352524, (case), Lot Numbers: 23EMB405, 23IMH248.
Amount recalled
1921 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 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.