MediNatura Initiates Nationwide Recall of ReBoost Nasal Spray Due to Microbial Contamination

MediNatura New Mexico, Inc. is initiating a voluntary nationwide recall of a specific lot of its ReBoost Nasal Spray due to the presence of yeast, mold, and microbial contamination, including a species identified as Achromobacter, at levels exceeding acceptable specifications. The U.S. Food and Drug Administration has been informed of this recall, which impacts consumers across the country who may have purchased the product.

The recalled product is a homeopathic nasal spray intended to provide temporary relief from symptoms such as nasal congestion, sinus headache and pressure, postnasal drip, sneezing, runny nose, and nasal itching. The nasal spray is packaged in a 0.68 fl oz (20mL) bottle, which is then housed in a white and yellow carton. Consumers can identify the affected product by its National Drug Code (NDC) number 62795-4005-9 and Universal Product Code (UPC) 787647 10186 3. The specific lot number subject to this recall is 224268, with an expiration date of December 2027.

The presence of microbial contamination presents a potential health risk, particularly to individuals with compromised immune systems. According to the company’s announcement, there is a reasonable probability that adverse health consequences, including life-threatening infections, could occur if immuno-compromised individuals use the contaminated product. As of the announcement date, MediNatura has not reported any adverse events associated with this particular recall.

ReBoost Nasal Spray was distributed nationwide through both retail establishments and online sales, including directly from the company’s website, medinatura.com. The company is advising all consumers to cease using the affected ReBoost product immediately.

Consumers who purchased the recalled nasal spray directly from MediNatura New Mexico, Inc. are instructed to contact the company via email at recall@medinatura.com to arrange for a refund. For those who purchased the product from retailers, the company recommends returning it to the place of purchase for a refund.

Individuals with questions regarding this recall can reach MediNatura New Mexico, Inc. by phone at 800-621-7644 or by email at recall@medinatura.com. The company is available to address inquiries Monday through Friday, between 8:00 AM and 5:00 PM Mountain Standard Time.

Consumers who have experienced any health issues that they believe may be related to the use of this nasal spray are urged to consult with their physician or healthcare provider. The FDA also encourages consumers to report any adverse reactions or quality concerns experienced with this or any other drug product through its MedWatch Adverse Event Reporting program. Reports can be submitted online via the FDA’s website, or by mail or fax using a downloadable form available on the FDA’s website.

Article by Mel Anara, based upon information from MediNatura New Mexico, Inc.

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