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FDA
Food and Drug Administration · Recall Z-3121-2026 · Aug 11, 2026

Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A

Medline Industries, LP

The hazard

The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death. FDA Class I recall.

The remedy

Follow FDA guidance

About this recall

Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model 1) DYKMBNDL199AModel UDI-DI: 10193489848540(each)Model 40193489848541(case)Model Lot Number: 24HBH109Model 2) DYKMBNDL199AModel Lot Number: 24HBM182Model 3) DYKMBNDL199AModel Lot Number: 24HBS365UPC 10193489848540UPC 40193489848541

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.