Data Foundry

Medical device recalls 2025

Cardinal Health Presource Kits: 1 ) KIT — Class II medical device recall Z-0911-2025

Ongoing recall by Cardinal Health 200, LLC, reported 2025-01-22, distributed nationwide. Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.

Recall numberZ-0911-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCardinal Health 200, LLC, Waukegan, IL, United States
Recall initiated2024-11-08
Classified2025-01-15
Reported by FDA2025-01-22
DistributedNationwide (US)
Countries outside the USCA, SA
Quantity512,786 units
Reason classessterility
UPC / GTIN / UDI-DI10195594888015, 10197106474570, 10888439587074, 50195594888013, 50197106474578, 50888439587072
Lot numbers21K3110, 22D1239, 23F1430, 23J2297, 24C0657, J1896M, J3987C, J43U76, J46C02, J4952G, J74A30, J8064Z, J8123Z, J84K03

Product

Cardinal Health Presource Kits: 1 ) KIT, MAJOR ORAL SURGERY, Catalog Number: PGDHMOWOE; 2 ) ORP DENTAL PACK , Catalog Number: SENHDDPVCH; 3 ) ORP DENTAL PACK, Catalog Number: SENHDDPVCI

Reason for recall

Potential 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-0911-2025. 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.