Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141
Summary
The FDA issued a Class II for Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per m by SterRx, LLC. Reason: Lack of Assurance of Sterility.
Details
Source
Drug Recall
External ID
D-0768-2021
Action Date
2021-09-01
Status
Terminated
Category
drug
Product Description
Sodium Bicarbonate in 5% Dextrose Injection, 150 mEq per 1,000 mL (12.6 mg per mL), 1,000 mL bags, Rx only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903
Lot/Code Info: Lot Numbers: BTW, exp. date 03/08/22 BUI, exp. date 03/16/22
Quantity Affected: 3378 bags
Reason for Recall
Lack of Assurance of Sterility
Distribution
Nationwide in the US
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-10
Company
Plattsburgh, NY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 58 drug recalls issued in the same week, part of 272 drug-related FDA actions this month.
SterRx, LLC has 35 FDA actions in our database, including 35 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (SterRx, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SterRx, LLC have FDA actions?
SterRx, LLC has 35 FDA actions in our database, including 35 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0768-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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