Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
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 (sterile medical device) where injury has not yet been reported, fitting the 'High' severity criteria for potential infection risk without confirmed illness.
Plain-English summary
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains, 10FR W/Trocar. These are sterile, single-use medical devices used to remove exudates from surgical wound sites. The recall is due to a potential compromise in the product's seal, which may affect the sterility of the package contents.
The use of these impacted products could result in an increased risk of infection. The affected products are identified by Catalog Number SU130-0323 and specific lot numbers: 1161366, 1161473, 1161603, 1161604, 1161605, and 1170033. The products were distributed nationwide.
Healthcare providers and facilities should stop using the affected lots and contact Cardinal Health 200, LLC for further instructions or replacement. Consumers should not use these products if they have them in their possession.
The recalled product
- Product
- Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/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 is a rad
- 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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