Navilyst Medical Recalls NAMIC Convenience Kits Due to Sterility Concerns
Navilyst Medical is recalling 2 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased 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 (sterility breach leading to infection) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Navilyst Medical, Inc. is recalling 2 units of NAMIC Convenience Kits, specifically the ANGIO DOUBLE SPIKE KIT (UPN H965603028111, REF/Catalog No. 600302811, Lot 4798703). These sterile, prescription-only devices are intended for use in Fluid Management and/or Invasive Pressure Monitoring Systems.
The recall was initiated because the labeled expiration dating of the affected product is not fully supported by shelf life verification testing. This deficiency may result in a sterility breach. The use of a Fluid Management Convenience Kit where sterility has been breached may result in an increased risk of infection.
The affected units were distributed worldwide, including the United States, Canada, and Guam. Consumers and healthcare providers should stop using the affected products and contact Navilyst Medical for further instructions.
The recalled product
- Product
- NAMIC Convenience Kit, ANGIO DOUBLE SPIKE KIT, UPN H9656003028111, REF/Catalog No. 600302811, STERILE, Rx ONLY --- For single use only. --- Device Listing Number D136683. NAMIC Convenience Kits are intended to be used in Fluid Management and/or Invasive Pressure Monitoring Sy
- Manufacturer
- Navilyst Medical, Inc
- Affected units
- 2
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 (1)
- Lot 4798703
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 60 recalled by Navilyst Medical, Inc 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 60 products in this recall →Related recalls
Same manufacturer · Navilyst Medical, Inc
See all →- HighNavilyst Medical Recalls NAMIC Convenience Kits Due to Sterility Concerns
FDA (Devices) · 2015-03-04
- HighNavilyst Medical Recalls NAMIC Convenience Kits Due to Sterility Concerns
FDA (Devices) · 2015-03-04
- HighNavilyst NAMIC Convenience Kits Recalled for Sterility Concerns
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- HighNavilyst Medical Recalls NAMIC Convenience Kits Due to Sterility Concerns
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- HighNavilyst Medical Recalls NAMIC Convenience Kits Due to Sterility Concerns
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