MEDLINE convenience kits labeled as: 1) MINOR SINGLE recall
MEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3) MAJOR BASIN PACK, REF DYNJ59816A…
Why was MEDLINE convenience kits labeled as: 1) MINOR SINGLE 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
1) REF DYNJ37698L: UDI/DI 10195327435523 (each) 40195327435524, (case), Lot Numbers: 23KMG076, 24AMA944, 24FMA911; 2) REF DYNJ50123D: UDI/DI 10195327201999 (each) 40195327201990, (case), Lot Numbers: 23FBP789, 24ABG308, 24BBQ467, 24DBP157; 3) REF DYNJ59816A: UDI/DI 10195327331573 (each) 40195327331574, (case), Lot Numbers: 23GBR142, 23IBJ642, 23LBD170, 23LBM241; 4) REF DYNJ68217A: UDI/DI 10195327352523 (each) 40195327352524, (case), Lot Numbers: 23EMB405, 23IMH248.
- Product
- MEDLINE convenience kits labeled as: 1) MINOR SINGLE BASIN PACK, REF DYNJ37698L; 2) BASIN PACK, REF DYNJ50123D; 3) MAJOR BASIN PACK, REF DYNJ59816A…
- Recalling firm
- Medline Industries, LP
- Quantity
- 1921 kits
- Distribution
- US Nationwide distribution.
- Recall date
- November 26, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)