FDAClass IIJune 10, 2015

0.9% Sodium Chloride Injection recall

0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.

Why was 0.9% Sodium Chloride Injection recalled?

Incorrect expiration date on label

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

CODES: KH04103, KH04104, KH04105

Product
0.9% Sodium Chloride Injection, USP, Flush Syringe, 10 mL in 12 mL, Sterile, Rx only, Code No. 2T0806 Usage: Flush syringe.
Recalling firm
MRP, LLC dba AMUSA
Quantity
200,000 units
Distribution
US Distribution in states of:OH, PA, AL, IL, TN, and CT.
Recall date
June 10, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls