Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

0.9% Sodium Chloride Injection Recalled by Amsino Medical USA Due to Mislabeling

Date: August 15, 2012
Company: Amsino Medical USA
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Amsino Medical USA directly.

Affected Products

0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 3 mL in 12 mL Single Use Syringe, Rx only, List no. 1078-33, made in Nashville, TN, manufactured for Hospira, Inc., Lake Forest, IL 60045 USA. Flush syringe.

Quantity: 196,400 units

Why Was This Recalled?

One lot of 0.9% Sodium Chloride Flush syringe, 3 mL in 12 mL may be mislabeled as 0.9% Sodium Chloride Flush syringe, 10 mL in 12 mL.

Where Was This Sold?

Distributed to one customer in Illinois.

About Amsino Medical USA

Amsino Medical USA has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report