Reported Aug 9, 2017 · Terminated
8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira,…
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?
- 8.4% Sodium Bicarbonate Inj., USP 50 mL Single-dose, 50 mEq (1 mEq/mL) 4.2 grams (84 mg/mL), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA
- NDC0409-6625-02
- Lot codes and dates
38 of 38 products
Products covered by this recall # Product as published 1 Lot: 72109EV Exp. 12/01/2018 2 Lot: 72110EV Exp. 12/01/2018 3 Lot: 72112EV Exp. 12/01/2018 4 Lot: 72113EV Exp. 12/01/2018 5 Lot: 72114EV Exp. 12/01/2018 6 Lot: 73068EV Exp. 01/01/2019 7 Lot: 73071EV Exp. 01/01/2019 8 Lot: 73072EV Exp. 01/01/2019 9 Lot: 73224EV Exp. 01/01/2019 10 Lot: 73225EV Exp. 01/01/2019 11 Lot: 73230EV Exp. 01/01/2019 12 Lot: 73231EV Exp. 01/01/2019 13 Lot: 73232EV Exp. 01/01/2019 14 Lot: 73233EV Exp. 01/01/2019 15 Lot: 73234EV Exp. 01/01/2019 16 Lot: 73235EV Exp. 01/01/2019 17 Lot: 73236EV Exp. 01/01/2019 18 Lot: 73298EV Exp. 01/01/2019 19 Lot: 74058EV Exp. 02/01/2019 20 Lot: 74104EV Exp. 02/01/2019 - Amount recalled
- 91,483,150 50 mL 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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