Cardinal Health Recalls Presource Packs with Potential Lubricant Contamination
Cardinal Health is recalling Presource Packs containing CliniClean Pericare Wipes due to potential lubricant contamination that may cause localized skin effects.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text describes potential localized skin effects (irritation, erythema, mild inflammation) without reporting any hospitalizations or significant injuries, fitting the Moderate severity criteria for low-risk contamination or voluntary precautionary recalls.
Plain-English summary
Cardinal Health 200, LLC is recalling Presource Packs containing CliniClean Pericare Wipes within BD Urinary Catheter Trays. The specific product affected is the KIT,GYN LAPAROSCOPY DH, Catalog Number PBOCGLN17, with Lot Number NGKV3390. The recall involves 36 units that were distributed nationwide in the United States.
The recall is being conducted because the CliniClean Pericare Wipes within the trays may 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 potential effects include irritation, erythema, or mild inflammation.
Healthcare facilities and consumers who have this specific product should stop using it and contact Cardinal Health for further instructions or a refund. The recall is classified as Class II by the FDA, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 36
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- 1) PBOCGLN17
- UDI-DI: 10198956345133(each)
- 50198956345131(case)
- Lot Number: NGKV3390
Distribution
Distributed nationwide across the United States.
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