0.9% Sodium Chloride Injection USP recall: Sterility Concern
0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation…
Why was 0.9% Sodium Chloride Injection USP recalled?
Lack of Assurance of Sterility: potential for leaking containers which lacks the assurance of sterility.
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 #: P337857, Exp 07/31/16
- Product
- 0.9% Sodium Chloride Injection USP, MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation…
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 282,080 bags
- Distribution
- Nationwide and Puerto Rico
- Recall date
- June 1, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)