The Recall Desk
HighFDA (Devices)·Z-0520-2026·Announced 2025-11-26

Basin packs recalled over smoke pencils that may activate unprompted

Medline is recalling 1,921 basin convenience packs containing SafeAir Smoke Evacuation Pencils, after Stryker expanded its recall of the pencils by 47 lots.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Scored 3 under the risk-of-harm criterion: an electrosurgical pencil that can activate without input or stay active is a burn hazard, and no injuries are reported.

Plain-English summary

Medline convenience kits containing SafeAir Smoke Evacuation Pencils are being recalled, including MINOR SINGLE BASIN PACK (REF DYNJ37698L), BASIN PACK (REF DYNJ50123D), MAJOR BASIN PACK (REF DYNJ59816A) and OSC BASIN PACK (REF DYNJ68217A).

Stryker Instruments has expanded the scope of its recall of SafeAir Smoke Evacuation Pencils, first initiated in October 2024, adding an additional 47 lots. The initial recall was due to the potential for the product to activate without manual input when plugged into a power source, or to remain active after the buttons are released.

The recall covers 1,921 kits, including UDI/DI 10195327435523 for each unit and 40195327435524 for the case, with lots including 23KMG076 and 24AMA944. The product was distributed nationwide in the United States. The FDA has classified the action as Class II.

An electrosurgical pencil that activates on its own or stays live is a burn hazard in the operating field. The enforcement record reports no injuries. Facilities should quarantine affected lots and follow Medline's instructions.

The recalled product

Product
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.
Manufacturer
Medline Industries, LP
Category
Medical Device — Surgical kit
Hazard
Affected units
1,921

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (18)

  • 1) REF DYNJ37698L: UDI/DI 10195327435523 (each) 40195327435524
  • (case)
  • Lot Numbers: 23KMG076
  • 24AMA944
  • 24FMA911
  • 2) REF DYNJ50123D: UDI/DI 10195327201999 (each) 40195327201990
  • Lot Numbers: 23FBP789
  • 24ABG308
  • 24BBQ467
  • 24DBP157
  • 3) REF DYNJ59816A: UDI/DI 10195327331573 (each) 40195327331574
  • Lot Numbers: 23GBR142
  • 23IBJ642
  • 23LBD170
  • 23LBM241
  • 4) REF DYNJ68217A: UDI/DI 10195327352523 (each) 40195327352524
  • Lot Numbers: 23EMB405
  • 23IMH248.

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 20 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 20 products in this recall →

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Same manufacturer · Medline Industries, LP

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Same hazard · unintended activation

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