Amsino Medical USA: Medical Device Recall in 2012 - (Recall #: Z-2393-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: August 15, 2012

Date Posted: September 26, 2012

Recall Number: Z-2393-2012

Event ID: 63105

Reason for Recall:

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.

Status: Terminated

Product Quantity: 196,400 units

Code Information:

KH03752

Distribution Pattern:

Distributed to one customer in Illinois.

Voluntary or Mandated:

Voluntary: Firm initiated