Cardinal Health 200, LLC Recalls

28 recalls on record in the United States

drugs: 1 medical: 27
medical Class II
2026-04-08

Cardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock,

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.

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drugs Class I
2026-03-25

Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 c

Non-Sterility: microbial contamination identified as Paenibacillus phoenicis

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) ENT TRAY

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) HARMONIZED SPINE VCH PHC

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) KIT, MER NEURO BACK

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) CHI STD NEURO CRANI OPT 2

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) SEPTO RHINO PACK

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-08-19

Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) BASIC PACK

Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

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medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-09

Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

View recall details →

medical Class II
2026-09-30

Cardinal Health 200, LLC recalls Presource Convenience Kits: 1) KIT, PRE OP

The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient harm or may lead to localized skin or soft tissue infection. Less commonly, systemic infection or other infectious complications may occur.

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medical Class II
2026-09-30

Cardinal Health 200, LLC recalls Presource Convenience Kits: 1) KIT, USGPIV

The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient harm or may lead to localized skin or soft tissue infection. Less commonly, systemic infection or other infectious complications may occur.

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medical Class II
2026-10-07

Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tu

The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.

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medical Class II
2026-10-07

Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tu

The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.

View recall details →

medical Class II
2026-10-07

Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tu

The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.

View recall details →

medical Class II
2026-10-07

Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tu

The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.

View recall details →