0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc. Bethlehe
Summary
The FDA issued a Class II for 0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 026 by B. Braun Medical, Inc.. Reason: Lack of sterility assurance: Bags have the potential to leak..
Details
Source
Drug Recall
External ID
D-0076-2023
Action Date
2022-12-14
Status
Terminated
Category
drug
Product Description
0.9% Sodium Chloride Injection USP 1000 mL Single-dose container Rx only NDC 0264-5802-00 B. Braun Medical Inc. Bethlehem, PA 18018-3524 USA 1-800-227-2862
Lot/Code Info: Lot: 0061832446 Exp. 31 Oct 2024
Quantity Affected: 756 bags
Reason for Recall
Lack of sterility assurance: Bags have the potential to leak.
Distribution
FL, NJ, PA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-25
Company
Allentown, PA
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 19 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
B. Braun Medical, Inc. has 282 FDA actions in our database, including 269 recalls and 13 clearances.
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 (B. Braun Medical, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does B. Braun Medical, Inc. have FDA actions?
B. Braun Medical, Inc. has 282 FDA actions in our database, including 269 recalls and 13 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0076-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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