# Major Recall Alert: Lactated Ringer’s Injection, E7500, 1L Recalled Due to Products Found to Contain Particulate Matter in Solution
B. Braun Medical Inc. has recently issued a voluntary, nationwide recall of two lots of **Lactated Ringer’s Injection, E7500, 1L** due to the presence of particulate matter in the solution. This recall affects distributors, hospitals, and healthcare facilities across the United States. Here’s everything you need to know about this important recall and the steps you need to take to ensure patient safety.
## Why This Recall is Important
When it comes to intravenous (IV) solutions, safety and sterility are paramount. Unfortunately, B. Braun Medical discovered that certain lots of their popular **Lactated Ringer’s Injection** may contain **particulate matter**—tiny particles identified as cellulose and stearates, with traces of inorganic materials like copper.
If particulates are infused into the bloodstream, especially intravenously, they can cause life-threatening complications, including:
- **Pulmonary emboli**: Blockage in the pulmonary blood vessels, leading to respiratory emergencies.
- **Blood vessel occlusion**: Blockages in blood flow, possibly resulting in tissue death or organ damage.
- **Phlebitis**: Inflammation of veins that may cause clotting.
- **Organ dysfunction**: The introduction of foreign materials into the circulatory system can trigger immune responses and lead to severe complications like hemolysis (breakdown of red blood cells).
While no adverse events have been reported to date, the recall has been issued as a proactive measure to safeguard public health. Failure to address the issue could lead to severe impact and delays in medical care.
## Details of the Recall
Here’s a breakdown of the important details you need to know:
- **Product Name**: Lactated Ringer’s Injection, USP, E7500, 1L
- **Manufacturer**: B. Braun Medical Inc.
- **Reason for Recall**: Products were found to contain particulate matter in the solution.
- **Lot Numbers**: Affected product can be identified by product code **E7500** or **NDC 0264-7750-07**.
- **Intended Use**: This IV solution is used for hydration and as a source of electrolytes in adults and pediatric patients.
- **Distribution**: Nationwide, sent to distributors, hospitals, and healthcare facilities.
B. Braun is actively contacting affected customers and providing an **Urgent Pharmaceutical Recall Acknowledgement** form to process returns.
For more information, visit the official [FDA recall page](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-inc-issues-voluntary-nationwide-recall-lactated-ringers-injection-1l-e7500-due).
## What You Should Do
If you are in possession of this product or believe your facility has been affected, here’s what to do immediately:
- **Stop using affected products**: Discontinue the use of all Lactated Ringer’s Injection 1L products under recall.
- **Contact B. Braun**: Reach out to the company by emailing **recalls@bbraunusa.com** or calling **844-903-6417** (Monday to Friday, 8:00 am to 5:00 pm EST).
- **Report Adverse Effects**: If you or a patient has experienced adverse reactions, report it to the **FDA's MedWatch Adverse Event Reporting Program** online or via mail/fax.
Hospitals and distributors are also encouraged to follow B. Braun’s instructions for product return and replacement.
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Your safety is our top priority. If you have concerns related to Lactated Ringer's Injection or other recalled products, consult a healthcare provider immediately. Stay vigilant and informed for better health and peace of mind!