0.9% Sodium Chloride Injection recall: Particulate Matter
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Why was 0.9% Sodium Chloride Injection recalled?
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
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 #: 25-037-JT*, Exp 1JAN2015, Note: the lot number may be followed by 01 or 90
- Product
- 0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
- Recalling firm
- Hospira Inc.
- Quantity
- 691,356 containers
- Distribution
- Nationwide
- Recall date
- August 14, 2013
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)