Data Foundry

Medical device recalls 2025

Cardinal Health Presource Kits: 1) KIT — Class II medical device recall Z-1133-2025

Ongoing recall by Cardinal Health 200, LLC, reported 2025-02-19, distributed nationwide. Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.

Recall numberZ-1133-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCardinal Health 200, LLC, Waukegan, IL, United States
Recall initiated2024-11-08
Classified2025-02-10
Reported by FDA2025-02-19
DistributedNationwide (US)
Countries outside the USCA, SA
Quantity973,785 units
Reason classessterility
UPC / GTIN / UDI-DI10197106527009, 10197106628096, 10197106732311, 50197106527007, 50197106628094, 50197106732319
Lot numbers6701856, 7160530, 7266123, 7331357, 7333452, 7333453, 7350003
Model numbersPB4FRHWFA, PB4FRHWFB, PB4FRHWFC

Product

Cardinal Health Presource Kits: 1) KIT,ROBOTIC HYSTERECTOMY, Catalog Number:PB4FRHWFA; 2) KIT,ROBOTIC HYSTERECTOMY, Catalog Number:PB4FRHWFB 3) KIT,ROBOTIC HYSTERECTOMY, Catalog Number:PB4FRHWFC

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1133-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.