Cardinal Health 200 recalls

Cardinal Health 200 has 290 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 14 Oct 2026. 154 are still ongoing. 27 were reported in the last 12 months.

Total recalls290since 2016
Last 12 months27reported
Class I3211% of total
Ongoing154latest 14 Oct 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 32 11%Class II 258 89%Class III 0 0%

Why cardinal health 200 is recalled

By year

Ongoing cardinal health 200 recalls

154 active

All cardinal health 200 recalls, newest first

290 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPresource Packs containing Medtronic Microstream Components recalledCardinal Health 200Device MalfunctionIL
DeviceCLASS IIPresource Packs Containing Stryker StrykeFlow PS recalledCardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Packs Containing Stryker StrykeFlow PS recalledCardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Packs Containing Stryker StrykeFlow PS recalledCardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Packs Containing Stryker StrykeFlow PS recalledCardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Convenience Kits: KIT, Usgpiv recalled by Cardinal Health 200Cardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Convenience Kits: KIT, PRE OP recalled by Cardinal Health 200Cardinal Health 200Packaging DefectsNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200Foreign MaterialNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IIPresource Packs Containing CliniClean Pericare Wipes within recalledCardinal Health 200OtherNationwide
DeviceCLASS IICardinal Health Presource Kits: Basic Pack recalledCardinal Health 200OtherNationwide
DeviceCLASS IICardinal Health Presource Kits: Septo Rhino Pack recalledCardinal Health 200OtherNationwide
DeviceCLASS IICardinal Health Presource Kits: Newnan Smr Pack recalledCardinal Health 200OtherNationwide
DeviceCLASS IICardinal Health Presource Kits: Harmonized Spine Vch Phc Pack recalledCardinal Health 200OtherNationwide
DeviceCLASS IICardinal Health Monoject Tuberculin Syringe Luer Lock recalledCardinal Health 200Packaging DefectsNationwide
DrugCLASS IWebcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply recalledCardinal Health 200SterilityNationwide
DeviceCLASS IIChest Drainage Units and Accessories recalled by Cardinal Health 200Cardinal Health 200Device MalfunctionNationwide
DeviceCLASS IIChemoPlus gowns recalled by Cardinal Health 200Cardinal Health 200Labeling ErrorsNationwide
DeviceCLASS II266122 Salem Sump" Stomach Tube, Dual Lumen recalledCardinal Health 200Device MalfunctionNationwide
DeviceCLASS II8888264911E ENFit" Salem Sump" PVC Tube 8888264929E ENFit" recalledCardinal Health 200Device MalfunctionNationwide
DeviceCLASS II266197 Salem Sump" Anti-Reflux Valve CE Marked recalledCardinal Health 200Device MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.