# Nasal Spray Recall: Over 40,000 Bottles Pulled for Bacterial Contamination – What You Need to Know
A significant health alert has been issued affecting consumers across the country. In a move to protect public safety, **more than 40,000 bottles of nasal spray have been recalled nationwide due to bacteria contamination**. The voluntary recall, initiated by the manufacturer and announced by the U.S. Food and Drug Administration (FDA), involves a popular over-the-counter product found in many homes. This contamination poses a serious health risk, especially to vulnerable individuals.
If you use a daily nasal spray for allergies or sinus relief, this news is critical. This comprehensive guide will walk you through everything you need to know about this nasal spray recall: which product is affected, the specific dangers of the bacterial contamination, and the exact steps you should take if you have this product in your medicine cabinet.
## What Nasal Spray is Being Recalled?
The recall is specific to one product and one particular lot. It is essential to carefully check your products to see if they match the details below.
### Identifying the Specific Product
The recalled product is **ManukaGuard Allercleanse Nasal Spray**. The recall was initiated by the product’s distributor, NDS-USA LLC, after FDA testing discovered the presence of dangerous bacteria.
Here are the exact details to look for on the packaging to determine if your product is part of the recall:
* **Product Name:** ManukaGuard Allercleanse Nasal Spray
* **UPC Code:** 858631002128
* **Lot Number:** 2307012
* **Expiration Date:** 09/2026
The lot number and expiration date are typically printed on the bottom of the bottle or on the side of the box. If your nasal spray matches all of these identifiers, it is part of the contaminated batch and should not be used under any circumstances. The product was distributed nationwide through various retail stores and online e-commerce platforms.
## The Dangers of the Bacterial Contamination
The reason for this urgent recall is the discovery of contamination with *Burkholderia cepacia* complex (Bcc), a group of bacteria that can cause serious infections. While these bacteria pose a low risk to healthy individuals, they can be life-threatening for certain populations.
### What is Burkholderia Cepacia Complex (Bcc)?
*Burkholderia cepacia* complex is a group of bacteria commonly found in soil and water. When it contaminates a medical product, especially one administered directly into the nasal passages, it can bypass the body’s natural defenses. The moist environment of the sinuses can become a breeding ground for the bacteria, leading to infection.
Introducing these bacteria directly into the body through a contaminated nasal spray can lead to a range of illnesses, from mild skin infections to severe respiratory infections and even bloodstream infections (sepsis).
### Who is Most at Risk?
The primary concern with this **nasal spray recall due to bacteria contamination** is the elevated risk for vulnerable individuals. Using a product contaminated with Bcc can have severe consequences for:
* **Immunocompromised Individuals:** People with weakened immune systems due to conditions like HIV, cancer treatment, or organ transplants are highly susceptible to infection.
* **People with Chronic Lung Diseases:** Individuals with conditions such as cystic fibrosis (CF) or chronic obstructive pulmonary disease (COPD) are at an extremely high risk. Bcc can cause a rapid decline in lung function in CF patients, an illness known as “cepacia syndrome,” which can be fatal.
* **Hospitalized Patients:** Anyone with an underlying health condition or currently receiving medical care may have a reduced ability to fight off infection.
For the general, healthy population, the risk of a severe infection is lower. However, any use of a contaminated product is unsafe, and the potential for infection still exists.
### Potential Symptoms of a Bcc Infection
If you have used the recalled nasal spray and are concerned about a possible infection, watch for the following symptoms. They can vary depending on the type and location of the infection.
* Fever and chills
* Coughing or difficulty breathing
* Increased congestion or sinus pain
* Skin rash or abscesses
* General feeling of being unwell (malaise)
If you have used the recalled product and experience any of these symptoms, it is crucial to contact your healthcare provider immediately. Be sure to inform them about your potential exposure to *Burkholderia cepacia* from the contaminated nasal spray.
## I Have the Recalled Nasal Spray. What Should I Do Now?
Finding out that a product you trust is part of a recall can be unsettling. Fortunately, there are clear, simple steps to take to ensure your safety and address the issue.
### Step 1: Stop Using the Product Immediately
The first and most important step is to stop using the ManukaGuard Allercleanse Nasal Spray from the affected lot right away. Do not try to “use up” the bottle. Continued use increases your risk of exposure to the harmful bacteria.
### Step 2: Verify the Lot Number and Expiration Date
Carefully inspect the bottle and its packaging. Double-check that the lot number is **2307012** and the expiration date is **09/2026**. If it matches, proceed to the next step. If it does not match, your product is not part of this specific recall, but it is always good practice to stay informed about product safety.
### Step 3: Safely Dispose of the Product
Do not simply throw the bottle in the trash where it could be picked up by someone else. The FDA recommends securing the product in a sealed bag before disposing of it in your household garbage. This prevents accidental exposure.
### Step 4: Seek a Refund and Report Issues
The company, NDS-USA LLC, is advising consumers who have the recalled product to contact them for information on how to return it for a full refund. You can reach the company by:
* **Email:** [email protected]
* **Phone:** 1-800-916-1220
Additionally, if you have experienced any adverse reactions or health problems from using this product, you should report them. You can do this through the FDA’s MedWatch Adverse Event Reporting program online or by downloading a form to submit by mail or fax. This reporting helps the FDA track health issues related to medical products and take necessary action.
## Staying Informed About Product Safety
This recall of over 40,000 bottles of nasal spray is a stark reminder of the importance of consumer vigilance. While the FDA and manufacturers work to ensure product safety, contaminated products can sometimes reach the market. By staying informed, you play an active role in protecting your and your family’s health.
Check the FDA’s recall website regularly for the latest updates on drugs, medical devices, and other consumer products. Understanding the details behind recalls—why they happen and who is at risk—empowers you to make safe choices for your household. In this case, the prompt action regarding the **nasal spray recall and its bacteria contamination** helps prevent widespread illness, especially among those who are most vulnerable.
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