Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains
Cardinal Health is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and 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 (sterile medical device) where the hazard is a theoretical increase in infection risk due to compromised sterility, with no reported injuries or illnesses stated in the source text.
Plain-English summary
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains, 19FR W/15FR Trocar. These sterile, single-use medical devices are used to remove exudates from surgical wound sites by collecting blood and fluids into a reservoir. The recall is due to a potential compromise in the product's seal, which may affect the sterility of the package contents.
The affected products are identified by Catalog Number JP-HUR195 and specific lot numbers: 1161199, 1161361, 1161458, 1161459, 1161594, 1161595, and 1161596. The products were distributed nationwide. Use of the impacted products could result in an increased risk of infection for patients.
Healthcare providers and facilities should stop using the affected lots and contact Cardinal Health 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, 19FR W/15FR 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
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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