MRP, LLC dba AMUSA: Medical Device Recall in 2015 - (Recall #: Z-1709-2015)

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, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.

Product Classification:

Class II

Date Initiated: April 27, 2015

Date Posted: June 10, 2015

Recall Number: Z-1709-2015

Event ID: 71175

Reason for Recall:

Incorrect expiration date on label

Status: Terminated

Product Quantity: 200,000 units

Code Information:

CODES: KH04103, KH04104, KH04105

Distribution Pattern:

US Distribution in states of:OH, PA, AL, IL, TN, and CT.

Voluntary or Mandated:

Voluntary: Firm initiated