Heparin Sodium in 0.9% Sodium Chloride Injection recall: Subpotent
Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, Manufactured for Baxter…
Why was Heparin Sodium in 0.9% Sodium Chloride Injection recalled?
Subpotent Drug: Heparin raw material was found to have low potency
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 #: N003061; N003079; and N003087, Exp 2/29/2016
- Product
- Heparin Sodium in 0.9% Sodium Chloride Injection, 1000 USP Heparin Units, 500 mL in a VIAFLEX Plus Container, Rx only, Manufactured for Baxter…
- Recalling firm
- Baxter Healthcare Corp.
- Quantity
- 127,746 Viaflex Plus Container
- Distribution
- Nationwide
- Recall date
- December 3, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)