Reported Aug 9, 2017 · Terminated
Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial…
Hospira a Pfizer Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Hospira a Pfizer Company · 4285 N Wesleyan Blvd · Rocky Mount, NC · 27804-8612
Is this the product you have?
- Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
- Lot codes and dates
- a.)
- one vialLot: 72226EV Exp. 12/01/2018
- Lot72236EV Exp. 12/01/2018
- Lot75382EV Exp. 03/01/2019
- Lot75383EV Exp. 03/01/2019 b.) 25
- vial carton
Lot: 7538EVExp 03/01/2019
- Amount recalled
- 21,436,700 5mL single dose vials
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Lack of Sterility Assurance
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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