← See all good sense nasal brands. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.Perrigo is notifying our retail customers by phone, email or other communication with recall notification communications to arrange for the return of all recalled product.Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.Perrigo Company plc is dedicated to making lives better by bringing high quality and affordable selfcare products that consumers trust everywhere they are sold. Visit Perrigo online at Lyndsey Chmiel, Senior Manager, Global Investor Relations & Corporate Communications, (269) 673-9324, E-mail: A single non-fatal adverse event potentially associated with the issue was reported in the US during the time of the affected product distribution.The company has not received an increase in adverse event reports to date related to the recalled products.Both DDAVP Nasal Spray and Desmopressin Acetate Nasal Spray are indicated as antidiuretic replacement therapy to manage central cranial diabetes insipidus, as well as the temporary polyuria and polydipsia following head trauma or surgery in the pituitary region.Further, Stimate Nasal Spray is to treat patients with hemophilia A with Factor VIll coagulant activity levels greater than 5%, as well as patients with mild to moderate classic von Willebrand's disease (Type I) with Factor VIII levels greater than 5%. Ferring Pharmaceuticals US is recalling various nasal sprays citing superpotency or amounts of desmopressin higher than specified, the U.S. Food and Drug Administration announced in a statement.The recall involves all lots on the market of DDAVP Nasal Spray 10 mcg/0.1mL, Desmopressin Acetate Nasal Spray 10 mcg/0.1mL, and STIMATE Nasal Spray 1.5 mg/mL.According to the agency, the risks associated with higher than specified amounts of desmopressin relate to abnormally low levels of sodium in the blood, i.e., hyponatremia, which could eventually lead to seizure, coma, and death.Ferring identified the issue during routine testing. An official website of the United States government: When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. U.S. 51 ($2.88/Fl Oz) Get it as soon as Wed, Aug 12. Maximum Strength. From the WebMD Archives. The recall involves all lots on the market of DDAVP Nasal Spray 10 mcg/0.1mL, Desmopressin Acetate Nasal Spray 10 mcg/0.1mL, and STIMATE Nasal Spray 1.5 mg/mL. The Company is a leading provider of over-the-counter health and wellness solutions that enhance individual well-being by empowering consumers to proactively prevent or treat conditions that can be self-managed. A CVS store-brand nasal spray is being recalled because it could be contaminated, the Food and Drug Administration says.The affected product, CVS Health 12 Hour Sinus Relief Nasal … good sense nasal by L. Perrigo Company. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables.Ranitidine is an over-the-counter (OTC) and prescription product indicated for the relief of heartburn associated with acid indigestion and sour stomach and prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages.After regulatory bodies announced that ranitidine may potentially contain NDMA, Perrigo promptly began testing of its externally sourced ranitidine API (active pharmaceutical ingredient) and ranitidine-based products. By Valarie Basheda. Azelastine HCl Nasal Solution (Nasal Spray), 0.15% Generic to: Astepro® Quality, Affordable Self-Care Products™ Come work for a leading global self-care company.
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