Ultra Seal Corporation recalls Ephedrine Plus tablets due to manufacturing deviations. Check NDC 65193-320-24, lots 18M063 (exp 01/2022) and 19G076 (exp 09/2022).
cGMP deviations
Ultra Seal Corporation is recalling Ephedrine Plus tablets (24-count bottles) because of manufacturing quality control issues. This recall affects products with specific lot numbers and expiration dates that may not meet safety standards.
The recall is due to cGMP (Current Good Manufacturing Practice) deviations, which means the tablets were produced without following standard quality control procedures. This could potentially lead to inconsistent medication strength or safety issues, though the exact risk is not specified in the recall notice.
People who own or use Ephedrine Plus tablets with NDC 65193-320-24, lot numbers 18M063 (expiring January 2022) or 19G076 (expiring September 2022) are affected. Those using the product for respiratory issues may be at higher risk due to the medication's purpose.
Check the product label for NDC 65193-320-24, lot number 18M063 (expiring January 2022) or 19G076 (expiring September 2022). The product is sold by DMD Pharmaceuticals A, a division of Dickery Consumer Products, Inc.
Look for NDC 65193-320-24, lot numbers 18M063 (expiring January 2022) or 19G076 (expiring September 2022) on the packaging.
The recall is due to cGMP deviations in manufacturing, which could affect the product's safety and quality.
The official notice does not specify a remedy, so check the product label for the lot numbers and expiration dates to determine if it is affected.
The recall does not specify a risk of serious injury, so the danger level is unknown.
We’ve drafted a message you can send Ultra Seal Corporation to request your refund or repair — edit it as you like.
Subject: Recall D-0473-2022 — Ultra Seal Corporation Ultra Seal Corporation Hello, I own a Ultra Seal Corporation that is covered by recall D-0473-2022 from Ultra Seal Corporation. 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.
