RemedyRepack recalls 0.2 mg Desmopressin tablets due to subpotency. Affected products have specific NDC numbers and expiration dates. Consumers should contact the manufacturer for details.
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
RemedyRepack is recalling 0.2 mg Desmopressin Acetate tablets that were repackaged by them. The product was found to be subpotent, meaning it may not contain enough active ingredient to be effective as intended. This could lead to treatment failure for conditions like bleeding disorders.
The repackaged product was found to be subpotent, meaning it contains less active drug than it should. This could result in the medication not working properly for conditions like bleeding disorders. However, the risk is not severe enough to cause serious injury in normal use.
People who have a prescription for Desmopressin Acetate tablets from RemedyRepack Inc. and are using the recalled product. Those with bleeding disorders or related conditions are at higher risk of treatment failure.
Check for the product name 'Desmopressin Acetate Tablet, 0.2 mg, 100-count box' with NDC number 70518-3493-00. The expiration dates are February 24, 2023, or February 26, 2023.
Look for the NDC number 70518-3493-00 on the packaging to confirm if it's affected.
The product was found to be subpotent, so it may not work as intended. However, the recall does not indicate a risk of serious injury.
The recall does not specify a remedy, so contact RemedyRepack Inc. for further instructions.
Check for the NDC number 70518-3493-00 and expiration dates of February 24, 2023, or February 26, 2023.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0077-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0077-2023 from RemedyRepack. 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.
