Recall
FDAHealthJuly 6, 2026

Spectra Medical Devices, Llc — Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flus

⚠️ Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance. If the product sterility is compromised, patients may be exposed to microorganisms, endotoxins, or foreign matter. This may trigger inflammatory responses, infections, micro-clots, and organ failure.

Is this relevant to me?

Geography
CA, FL, NC, OK, TX, VA
Source agency
FDA
Category
Health
Published
July 6, 2026

Distributed in the United States to medical device kit packers in six (6) states - CA, FL, NC, OK, TX, VA.

What's affected?

Product
Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride Injection, 0.9%, USP 10mL Ampule Model/Catalog Number: AMPUL10MLK. Sodium Chloride Flush for IV tubing systems and indwelling intravascular access devices.
Lot code
Product

Additional details

Lot Code: Product codes: 1510-1 (individual ampule) / 1510-2 (carton) Lots: AB3005, AB3006, AB3007, AB3008, AB3009, AB3010, AB4001, AB4002, AB4003, AB4004, AB4005 AB4006, AB5001, AB5002, AB5003, AB5004, AB5005,AB5006, AB5007, AB5008 No individual UDI, as this product is used only within convenience kits.

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: TBD.

View original FDA notice →

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