Lower riskDrug recall · FDA · Published January 12, 2024
IntegraDose Vasopressin Recall: Subpotent Drug Risk
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.
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. Read more at govinfonow.com/recall/32883-integradose-vasopressin-recall-subpotent-drug-risk.
“IntegraDose Vasopressin Recall: Subpotent Drug Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32883-integradose-vasopressin-recall-subpotent-drug-risk. Based on FDA recall #D-0258-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0258-2024%22&limit=1).
The FDA announced on Jan. 12, 2024, that IntegraDose Compounding Services LLC is recalling Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride due to subpotent drug risks. The voluntary Class II recall affects 281 syringes distributed only in Minnesota.
How to tell if you have it
Brand: IntegraDose
Product: Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only
NDC: 71139-0190-1
Lot #: 20230921VAS-2
Exp. Date: 03/19/2024
Quantity: 281 syringes
Distribution: MN only
The hazard
The product is classified as a subpotent drug, meaning it may not contain the labeled amount of active ingredient. The FDA recorded this hazard for the recalled lot.
Context
GovInfoNow's records show IntegraDose Compounding Services LLC has 6 other recalls on record since Sept. 17, 2021. Other recent recalls of similar products include IntegraDose Vasopressin 2 Units/2mL Recall (May 18, 2026), IntegraDose Fentanyl Citrate Recall (May 12, 2026), and IntegraDose Oxytocin IV Solution Recall (Sept. 16, 2025). Other recent recalls of similar products include ImprimisRx Povidone Iodine Ophthalmic Solution Recall (Aug. 24, 2026), Baxter Vasopressin Injection Recall (Aug. 6, 2026), and Gasco Isopropyl Alcohol 70% Recall (May 29, 2026).
How to tell if you have this one
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.
Brand
IntegraDose
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the NDC number 71139-0190-1 and lot number 20230921VAS-2 on the product label.
Where it went and when
Where it was distributed
Distributed in Minnesota.
Listed by the agency
Not listed
FDA distribution: “MN only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA published this recall 19 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #D-0258-2024 (January 12, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0258-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.