FDAClass IIJune 24, 2015

T/S2 0.9% Sodium Chloride Injection recall: Labeling Error

T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush…

Why was T/S2 0.9% Sodium Chloride Injection recalled?

Incorrect labeling of the expiration date

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?

KH04090

Product
T/S2 0.9% Sodium Chloride Injection, USP, AMUSA Sterile Field Flush Syringe, 10 mL in 12 mL Single Use Syringe, Rx only, Part no. 2S0706 Usage: Flush…
Recalling firm
MRP, LLC dba AMUSA
Quantity
1,080 units (3 cases)
Distribution
US distribution to CA only.
Recall date
June 24, 2015
Classification
Class II
Status
Terminated
Agency
FDA (device)
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