IntegraDose recalls Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride with subpotent drug risk. Affected units have NDC 71139-0190-1, lot 20230921VAS-2, expiring 03/19/2024.
Subpotent Drug
IntegraDose is recalling Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride due to a subpotent drug hazard. This means the medication may not work as intended when used as prescribed, potentially leading to ineffective treatment.
The medication is subpotent, meaning it contains less active drug than it should. This could result in the treatment not working properly when used as directed, but does not cause immediate harm or injury.
Prescription patients using this specific Vasopressin product. Healthcare providers who dispensed the recalled units are most at risk of administering ineffective treatment.
Check for the NDC number 71139-0190-1 on the product label. The lot number is 20230921VAS-2 and the expiration date is March 19, 2024.
Look for the NDC number 71139-0190-1 and lot number 20230921VAS-2 on the product label.
The product has a subpotent drug hazard, meaning it may not work as intended when used as prescribed. It does not cause immediate harm but could lead to ineffective treatment.
Check for the NDC number 71139-0190-1 and lot number 20230921VAS-2 on the product label.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the product.
We’ve drafted a message you can send IntegraDose to request your refund or repair — edit it as you like.
Subject: Recall D-0258-2024 — IntegraDose IntegraDose Hello, I own a IntegraDose that is covered by recall D-0258-2024 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.