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Cardinal Health 200 Recalls
285 recalls on record · October 19, 2016 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK , Catalog Number: PN33NBMYD; 2) KIT,CHP BASIC NEURO
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2 , Catalog Number: CHIP99NC27; 2) CHI STD NEURO CRANI O
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRAN
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC PACK , Catalog Number: SOP30SPBCC
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
August 19, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT , Catalog Number: 21-4720B; 2) TRAY FAT GRAFT ADD
Hazard: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
April 8, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
Hazard: The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.
March 25, 2026DrugsFDA
Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Wa
Hazard: Non-Sterility: microbial contamination identified as Paenibacillus phoenicis
February 4, 2026Medical DevicesFDA
Cardinal Health 200, LLC recalls Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2.
Hazard: The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older. When used on infants, the CDU may not demonstrate tidaling/bubbling, which may confound the clinician's assessment of device functionality and lead to inadequate/inappropriate treatment/therapy, delay to treatment/therapy, and prolonged hospitalization.
December 17, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-
Hazard: Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 266122 Salem Sump" Stomach Tube, Dual Lumen with Anti-Reflux Valve,
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
October 29, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE 10FR 36IN 8888264929E EN
Hazard: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
June 18, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Kendall SCD Blended Comfort Sleeves Knee Length Small - For use with Kendall SCD SmartFlow SKU 84021B Kendall S
Hazard: Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
June 18, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Kendall SCD Comfort Sleeves Knee Length Small, Pediatric - For use with Kendall SCD SmartFlow, SKU 84021P Kendall
Hazard: Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
June 18, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls SCD Comfort Knee Length Small, SKU 84021; Kendall SCD Small Comfort sleeves when used with the Kendall SCD Smartflow Con
Hazard: Incorrect software logic may cause frequent E1 errors (system high pressure). Issue may cause delay in treatment or therapy.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160556; Umbilical Vessel Catheter 5 French dual lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160325; Umbilical Vessel Catheter 2.5 French single lumen
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
June 4, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Catalog No. 8888160119; Umbilical Vessel Catheter Insertion Tray with 2.5 and 5 French UVCs
Hazard: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) ACDF PACK, Catalog Number: SNEHBACSCA; 2) ACDF PACK, Catalog Number: SNEHBACSCB
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) OPHTHALMOLOGY ENDO DCR XTRS PK, Catalog Number:SEY30EYRVA; 2) OPHTHALMOLOGY ENDO DC
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.
February 19, 2025Medical DevicesFDA
Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) CHI STD SPINE OPTION 1, Catalog Number:CHIP99SP11; 2) CHI STD SPINE OPTION 1, Catalog
Hazard: Potential for endotoxin contamination in non-sterile surgical strips and patties in Presource Kits.