RecallHawk
Class II Recall

Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7

B. Braun Medical Inc

Summary

The FDA issued a Class II for Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medic by B. Braun Medical Inc. Reason: Lack of assurance of sterility: bags have the potential to leak...

Details

Source

Drug Recall

External ID

D-0431-2024

Action Date

2024-04-10

Status

Terminated

Category

drug

Product Description

Lactated Ringer's Injection USP, 1000mL, EXCEL CONTAINER, Rx only, B.Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7750-00

Lot/Code Info: Lot #: J3N023, Exp: 31 March 2026

Quantity Affected: 7,800 bags

Reason for Recall

Lack of assurance of sterility: bags have the potential to leak..

Distribution

Nationwide in the USA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-22

Company

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 61 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-0431-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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