The Recall Desk
ModerateFDA (Devices)·Z-0623-2025·Announced 2024-12-11

Medline Medical Convenience Kits Recall Due to Recalled Component

Medline is recalling certain medical convenience kits manufactured with SafeAir Smoke Evacuation Pencils that were previously recalled by Stryker. The recall affects 182 units distributed nationwide.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This recall is scored as Moderate (2) because it is a Class II medical device recall with no reported illnesses, injuries, or hospitalizations, and the specific hazard from the recalled component is not detailed in the FDA notice, making this a precautionary product recall.

Plain-English summary

Medline Industries, LP is recalling certain medical convenience kits because they were manufactured using lots of the SafeAir Smoke Evacuation Pencil, which was previously recalled by Stryker, the pencil manufacturer. The affected products include four product lines: ACETABULAR PACK-LF, LOCAL BASIC (two variants), and MINI LOCAL, with specific reference numbers and associated lot numbers provided by the manufacturer.

The recalled kits are distributed nationwide and total 182 units. Healthcare facilities and individuals that have received these kits should identify them using the reference numbers and lot numbers provided and cease use of the affected products.

Consumers and healthcare providers should contact Medline Industries for information on return, replacement, or proper disposal of the recalled kits.

The recalled product

Product
MEDLINE medical convenience kits labeled as: 1) ACETABULAR PACK-LF, REF DYNJ0572894I; 2) LOCAL BASIC, REF DYNJ34418L; 3) LOCAL BASIC, REF DYNJ34418M; 4) MINI LOCAL, REF DYNJ900287D
Manufacturer
MEDLINE INDUSTRIES, LP - Northfield
Category
Medical Device — Surgical Convenience Kits
Hazard
  • defective-component

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 (20)

  • 1) REF DYNJ0572894I
  • UDI/DI 10195327045975 (each) 40195327045976 (case)
  • Lot Numbers: 22EBV549
  • 22FBV442
  • 23ABU908
  • 22LBG711
  • 23CBJ089
  • 23BBM090
  • 23GBS959
  • 23JBG841
  • 2) REF DYNJ34418L
  • UDI/DI 10193489969276 (each) 40193489969277 (case)
  • Lot Numbers: 23CBT026
  • 23ABO601
  • 3) REF DYNJ34418M
  • UDI/DI 10195327384371 (each) 40195327384372 (case)
  • Lot Numbers: 23GBA504
  • 4) REF DYNJ900287D
  • UDI/DI 10193489798289 (each) 40193489798280 (case)
  • Lot Numbers: 23BBT640

Distribution

Distributed nationwide across the United States.

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