FDA Device recall Z-1131-2025

Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK, Catalog Number:SRIET0979N

FDA Device
Class II
ongoing
Published 2025-02-19

On 2025-02-19 the FDA classified a Class II recall of Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK, Catalog Number:SRIET0979N by Cardinal Health 200, citing potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1131-2025
Classification	Class II
Status	ongoing
Initiated	2024-11-08
Published	2025-02-19
Last updated	2026-09-13 11:57 UTC
Company	Cardinal Health 200
Distribution	US

Product

Cardinal Health Presource Kits: 1) LARYNGOSCOPY PACK, Catalog Number:SRIET0979N;

Reason

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

Identifiers

code_info	1) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4219A ; 2) SRIET0979N, UDI-D… 1) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4219A ; 2) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4678M ; 3) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J53W13 ; 4) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6277W ; 5) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J7904P ; 6) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J8491U ; 7) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6785Z ; 8) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6786D ; 9) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J9602P ; 10) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J96A00 ; 11) SRIET0979N, UD

code_info

1) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4219A ; 2) SRIET0979N, UDI-D…

1) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4219A ; 2) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J4678M ; 3) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J53W13 ; 4) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6277W ; 5) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J7904P ; 6) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J8491U ; 7) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6785Z ; 8) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J6786D ; 9) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J9602P ; 10) SRIET0979N, UDI-DI:10885425517206 (each) 50885425517204 (case), Lot Number: J96A00 ; 11) SRIET0979N, UD

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-1131-2025%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.