Device recall

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

FDA recall source

Recall number

Z-3121-2026

Event id

99669

Status

Ongoing

FDA classification

Class I

Recalling firm

Medline Industries, LP

Report date

Sep 23, 2026

Posted

Sep 14, 2026

Initiated

Aug 11, 2026

Center classification date

Sep 14, 2026

Product code

CAI

Device type

Circuit, Breathing (W Connector, Adaptor, Y Piece)

Reason

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.

Root cause

Nonconforming Material/Component

Quantity

12 kits

Code info

1) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBH109; 2) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBM182; 3) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBS365

Distribution

US Nationwide distribution.

Voluntary or mandated

Voluntary: Firm initiated

Location

Northfield, IL, United States