IntegraDose recalls Vasopressin 2 Units/2mL in 0.9% Sodium Chloride due to subpotent drug risk. Affected lots have specific NDC and expiration dates. Contact for remedy.
Subpotent Drug
IntegraDose is recalling Vasopressin 2 Units/2mL in 0.9% Sodium Chloride because it may be subpotent. This means the medication might not work as intended, which could affect treatment effectiveness.
Subpotent drugs have reduced effectiveness compared to the intended strength. This could lead to inadequate treatment if the medication doesn't work as prescribed.
Patients using this specific Vasopressin product for medical treatment. Healthcare providers who administered the medication are most at risk.
Check for the NDC number 71139-0190-1 on the product label. Look for lot numbers 20260327VAS-3 (expires 05/26/2026) or 20260320VAS-3 (expires 05/19/2026).
Verify the NDC number 71139-0190-1 and lot numbers 20260327VAS-3 or 20260320VAS-3 on the product label.
The recall states it may be subpotent, meaning it could be less effective than intended. Do not use if you have the specific lot numbers listed.
Check the product label for the NDC number 71139-0190-1 and lot numbers 20260327VAS-3 or 20260320VAS-3. If you have these, contact IntegraDose for instructions.
Look for the NDC number 71139-0190-1 and lot numbers 20260327VAS-3 (expires 05/26/2026) or 20260320VAS-3 (expires 05/19/2026) on the product label.
We’ve drafted a message you can send IntegraDose to request your refund or repair — edit it as you like.
Subject: Recall D-0593-2026 — IntegraDose IntegraDose Hello, I own a IntegraDose that is covered by recall D-0593-2026 from IntegraDose. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.