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FDA
Food and Drug Administration · Recall Z-3122-2026 · Aug 11, 2026

Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Number: DYNDA1080

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) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Number: DYNDA1080

Affected identifiers

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

Model 1) CDS840396YModel UDI-DI: 10195327574932(each)Model 40195327574933(case)Model Lot Number: 24FBJ654Model 2) CDS983672OModel UDI-DI: 10195327207625(each)Model 40195327207626(case)Model Lot Number: 24FBM444Model 3) CDS983672OModel Lot Number: 24HBJ581Model 4) DYNDA1080Model UDI-DI: 10884389388679(each)Model 40884389388670(case)Model Lot Number: 24HBT102UPC 10195327574932UPC 40195327574933UPC 10195327207625UPC 40195327207626UPC 10884389388679UPC 40884389388670

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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.