Cardinal Health Presource Kits: 1 ) TRIPLE ENDO PACK recalled over sterility concerns
- Recall date
- November 8, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1 ) TRIPLE ENDO PACK, Catalog Number: SBAOCTEHH1:; 2 ) TRIPLE ENDO PACK, Catalog Number…
- Recall number
- Z-0909-2025
- FDA classification
- Class II
- Brand / firm
- Cardinal Health 200, LLC
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of Canada, Saudi Arabia.
Why it was recalled
Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Cardinal Health Presource Kits: 1 ) TRIPLE ENDO PACK, Catalog Number: SBAOCTEHH1:; 2 ) TRIPLE ENDO PACK, Catalog Number: SBAOCTEHHA:; 3 ) RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERM5:; 4 ) RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERMO:; 5 ) RIVERSIDE SINUS ENDOSCOPY PK, Catalog Number: SEN15SERMP:;
Get recall alerts
Free email alert whenever Cardinal Health 200, LLC has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Cardinal Health 200, LLC