0.9% Sodium Chloride Injection USP recall: Sterility Concern
0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,
Why was 0.9% Sodium Chloride Injection USP recalled?
Lack of Assurance of Sterility: There is the potential for solution to leak from the administrative port to the fill tube seal.
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?
Lot Number 02-117-JT Exp. 02/13
- Product
- 0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,
- Recalling firm
- Hospira Inc.
- Quantity
- 325,056 bags
- Distribution
- Nationwide
- Recall date
- March 13, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)