Akorn recalls 0.005% Calcipotriene Topical Solution (Scalp Solution) due to potential delivery system defect preventing proper dispensing. Rx only, 60mL bottles manufactured by HI-TECH.
Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.
Akorn is recalling 0.005% Calcipotriene Topical Solution (Scalp Solution) because the delivery system might not work properly. This could mean the medication doesn't dispense as intended, which is important for people using it under a doctor's supervision.
The product may not dispense correctly, meaning the medication might not be delivered to the skin as intended. This could lead to ineffective treatment of skin conditions like psoriasis.
People with a prescription for this scalp solution who use it as directed. Those most at risk are individuals who rely on the medication for skin conditions.
Check for the 60 mL (2 fl. oz.) bottle labeled 'Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only'. The product was manufactured by HI-TECH PHARMACAL CO., INC. in Amityville, N.Y. with NDC 50383-732-02 and lot number 378440.
Verify the product label matches the description: 60 mL (2 fl. oz.) bottle, 'Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only'.
The recall states there's a potential defect that could prevent proper dispensing, but it doesn't indicate immediate safety risks. Consult your doctor for guidance.
Look for the 60 mL (2 fl. oz.) bottle with the label 'Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only' manufactured by HI-TECH PHARMACAL CO., INC. in Amityville, N.Y. with NDC 50383-732-02 and lot number 378440.
The recall doesn't specify a remedy, so contact your doctor or pharmacist for advice on whether to continue using the product.
We’ve drafted a message you can send Akorn to request your refund or repair — edit it as you like.
Subject: Recall D-1170-2022 — Akorn Akorn Hello, I own a Akorn that is covered by recall D-1170-2022 from Akorn. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
