Neut Bicarbonate ( ) Additive recalls

The FDA has published 1 recall involving Neut Bicarbonate ( ) Additive since 2017. The latest was reported on 9 Aug 2017. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2017

Last 12 months0reported

Class I00% of total

Ongoing0latest 9 Aug 2017

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why neut bicarbonate ( ) additive is recalled

Sterility1100%

Companies

Hospira a Pfizer1100%

By year

20171100%

All neut bicarbonate ( ) additive recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
9 Aug 2017Drug	CLASS II	Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution recalled	Hospira a Pfizer	Sterility	PR

Should you stop taking Neut Bicarbonate ( ) Additive?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.