Cardinal Health Recalls Presource Total Hip Kits Due to Airflow Risk
Cardinal Health is recalling 4,571 Presource Total Hip Kits because plastic packaging remnants may obstruct airflow in the filter.
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 I, which typically indicates a low risk of adverse health consequences, aligning with a Moderate severity score for a potential mechanical obstruction without reported injuries.
Plain-English summary
Cardinal Health, Medical Products & Services is recalling 4,571 Presource PBDS, Total Hip, Kit, Circulator units. The recall is due to a potential defect where outer plastic packaging on components may leave remnants in the filter if removed without disassembling the components, potentially causing an obstruction of airflow.
The affected kits are identified by Catalog Number PO24THGWG01 and Lots 966051 and 970753. These products were distributed in the states of Arkansas, Mississippi, South Carolina, and Tennessee.
Healthcare providers and consumers should stop using the affected kits and contact Cardinal Health for instructions on return or replacement.
The recalled product
- Product
- Presource PBDS, Total Hip, Kit, Circulator
- Manufacturer
- Cardinal Health, Medical Products & Services
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 4,571
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 (3)
- Catalog Number: PO24THGWG01
- Lots: 966051
- 970753
Distribution
Part of a larger recall action
This product is one of 14 recalled by Cardinal Health, Medical Products & Services under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 14 products in this recall →Related recalls
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- SevereCardinal Health Recalls Presource PBDS Kits Due to Airflow Obstruction Risk
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