MRP, LLC dba AMUSA: Medical Device Recall in 2015 - (Recall #: Z-2476-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.

Product Classification:

Class II

Date Initiated: July 2, 2015

Date Posted: September 2, 2015

Recall Number: Z-2476-2015

Event ID: 71735

Reason for Recall:

Procedures for the acceptance and control of in-process product have not been adequately established.

Status: Terminated

Product Quantity: 551 cases

Code Information:

KH04143,exp. 07/2016; KH04145, exp. 08/2016; KH04153, exp. 11/2016; KH04155, exp. 12/2016

Distribution Pattern:

Distributed in the states of CA. PA, VA, TX, MA, MD, WV, UT, FL, and TN.

Voluntary or Mandated:

Voluntary: Firm initiated