(NEXSTAR) — A New Mexico company has voluntarily recalled one lot of nasal spray sold nationwide after it was found to “contain yeast/mold and microbial contamination,” according to a notice shared by the Food and Drug Administration.
The notice, posted Wednesday, said MediNatura New Mexico, Inc. made the voluntary recall of some of its ReBoost Nasal Spray based on the findings.
Advertised uses for the homeopathic nasal spray include “temporarily relieve nasal congestion, sinus headache and pressure, postnasal drip, sneezing, runny nose, and nasal itching.”
Levels of Achromobacter detected in the nasal spray were “above specifications,” according to the recall. Achromobacter can cause infections, some of which can be difficult to treat because of its resistance to many antibiotics.
“There is a reasonable probability that adverse health consequences including life-threatening infections will occur with use of the product in the immuno-compromised population,” the recall notice reads, adding that there have not been “any reports of adverse events” thus far.
The recalled nasal spray was sold in 20mL bottles, which come in a white and yellow box. They are printed with the following numbers:
- NDC number: 62795-4005-9
- UPC: 787647 10186 3
- Lot number: 224268
- Expiration date: 12/2027
You can see an image of the packaging below:
The ReBoost Nasal Spray was distributed throughout the U.S., both at retailers and online through MediNatura’s website.
If you have a recalled bottle of ReBoost Nasal Spray, you are advised to stop using it and either return it to the store where it was purchased or contact MediNatura via email at recall@medinatura.com for a refund if it was bought online. Questions can also be directed to the MediNatura email address, or by calling 800-621-7644 between 8 a.m. and 5 p.m. MST, Monday through Friday.
The FDA recommends speaking with your physician or healthcare provider if you experience any problems while using the nasal spray.