B. Braun Medical, Inc. Issues Voluntary Nationwide Recall of Lactated Ringer’s Injection, 1L, E7500 Due to the Presence of Particulate Matter in Solution

Date

Apr 28, 2026

Company

B. Braun Medical Inc.

Brand

B. Braun

Product

Lactated Ringer’s Injection, E7500, 1L

Reason

Products were found to contain particulate matter in solution

Hazard

Other

Source

FDA

How to identify the product

• The product can be identified by product code E7500 or NDC 0264-7750-07.
• Product was distributed Nationwide to distributors, hospital, and healthcare facilities.
• Braun is notifying its distributors and customers by mail and is arranging for return of all recalled products.
• Consumers and distributors that have product which is being recalled should stop using and arrange for return of the product using the Urgent Pharmaceutical Recall Acknowledgement form provided by the company.

Product photos are on the official FDA page.

Official notice (FDA)

Facts are taken from the official notice. If anything here differs from it, the official notice is correct.