FDA Device recall Z-0912-2025

Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2

FDA Device
Class II
ongoing
Published 2025-01-22

On 2025-01-22 the FDA classified a Class II recall of Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2 by Cardinal Health 200, citing potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0912-2025
Classification	Class II
Status	ongoing
Initiated	2024-11-08
Published	2025-01-22
Last updated	2026-09-13 11:57 UTC
Company	Cardinal Health 200
Distribution	US

Product

Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2 ; 2 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH3 ; 3 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH4 ; 4 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH5 ; 5 ) STERILE LARYNGOSCOPY PACK, Catalog Number: SEN11LGUHB

Reason

Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.

Identifiers

code_info	Catalog Number SEN11LGUH2, UDI/DI 10195594093310 (EA)50195594093318 (CS), Lot Number J86T83 ; Catalog Number… Catalog Number SEN11LGUH2, UDI/DI 10195594093310 (EA)50195594093318 (CS), Lot Number J86T83 ; Catalog Number SEN11LGUH3, UDI/DI 10195594169626 (EA)50195594169624 (CS), Lot Number 5140349 ; Catalog Number SEN11LGUH4, UDI/DI 10195594230333 (EA)50195594230331 (CS), Lot Number 5405627 ; Catalog Number SEN11LGUH5, UDI/DI 10195594321871 (EA)50195594321879 (CS), Lot Number J6278U ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J43U76 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679G ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J74A30 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360

code_info

Catalog Number SEN11LGUH2, UDI/DI 10195594093310 (EA)50195594093318 (CS), Lot Number J86T83 ; Catalog Number…

Catalog Number SEN11LGUH2, UDI/DI 10195594093310 (EA)50195594093318 (CS), Lot Number J86T83 ; Catalog Number SEN11LGUH3, UDI/DI 10195594169626 (EA)50195594169624 (CS), Lot Number 5140349 ; Catalog Number SEN11LGUH4, UDI/DI 10195594230333 (EA)50195594230331 (CS), Lot Number 5405627 ; Catalog Number SEN11LGUH5, UDI/DI 10195594321871 (EA)50195594321879 (CS), Lot Number J6278U ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J43U76 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679G ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J74A30 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0912-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.