Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains
Cardinal Health is recalling specific lots of Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (sterility compromise leading to infection risk) where no specific injuries or illnesses have been reported in the source text, fitting the criteria for a High severity score.
Plain-English summary
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Hemaduct Silicone Round Drains, 10FR W/10FR Trocar. These are sterile, single-use medical devices used to remove exudates from surgical wound sites. The affected products are identified by Catalog Number JP-HUR101 and specific lot numbers listed in the recall notice.
The recall was initiated because the product's seal may be compromised, which could potentially compromise the sterility of the package contents. The use of these impacted products could result in an increased risk of infection for patients.
The affected products were distributed nationwide. Healthcare providers and facilities should check their inventory for the specific lot numbers listed in the recall and stop using any affected units. Consumers who have received these products should contact their healthcare provider for guidance.
The recalled product
- Product
- Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/10FR Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain i
- Manufacturer
- Cardinal Health 200, LLC
- Category
- Medical Device — Surgical Drains
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 recalled by Cardinal Health 200, LLC 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.
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