Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to CGMP Deviations: products were stored outside the drug...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Mckesson Medical-Surgical Inc. Corporate Office directly.
Affected Products
Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator, For temporary relief of mild symptoms of intermittent asthma, Preservative Free, Sterile, For Oral Inhalation Only, 30 vials per box, Nephron Pharmaceuticals Corporation, NDC 0487-2784-01.
Quantity: 1 box
Why Was This Recalled?
CGMP Deviations: products were stored outside the drug label specifications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Mckesson Medical-Surgical Inc. Corporate Office
Mckesson Medical-Surgical Inc. Corporate Office has 276 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report