Cardinal Health 200, LLC: Medical Device Recall in 2025 - (Recall #: Z-1127-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Cardinal Health Presource Kits: 1) KIT,NEURO LAMI,MD ANDERSON, Catalog Number:PN76LMM14; 2) KIT,NEURO LAMI,MD ANDERSON, Catalog Number:PN76LMMD9; 3) KIT,NEURO LAMI,MD ANDERSON, Catalog Number:PN76LMMDX;

Product Classification:

Class II

Date Initiated: November 8, 2024

Date Posted: February 19, 2025

Recall Number: Z-1127-2025

Event ID: 95947

Reason for Recall:

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

Status: Ongoing

Product Quantity: 973,785 total units

Code Information:

1) PN76LMM14, UDI-DI:10888439914467 (each) 50888439914465 (case), Lot Number: J8241D ; 2) PN76LMM14, UDI-DI:10888439914467 (each) 50888439914465 (case), Lot Number: J79Z55 ; 3) PN76LMMD9, UDI-DI:10888439651416 (each) 50888439651414 (case), Lot Number: J4220A ; 4) PN76LMMD9, UDI-DI:10888439651416 (each) 50888439651414 (case), Lot Number: J4220D ; 5) PN76LMMDX, UDI-DI:10888439401318 (each) 50888439401316 (case), Lot Number: J4953F ; 6) PN76LMMDX, UDI-DI:10888439401318 (each) 50888439401316 (case), Lot Number: J46C13 ;

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Canada, Saudi Arabia.

Voluntary or Mandated:

Voluntary: Firm initiated