“IntegraDose Vasopressin Syringes: Sub-potent Drug Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32853-integradose-vasopressin-syringes-sub-potent-drug-risk. Based on FDA recall #D-0325-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0325-2024%22&limit=1).
The FDA announced on Jan. 22, 2024, that IntegraDose Compounding Services LLC is recalling Vasopressin sterile syringes due to sub-potent drug risks. Owners should stop using the product immediately.
How to tell if you have it
Brand: IntegraDose
Product: Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe
The recall addresses the failure to maintain potency through the duration of the labeled expiration or beyond-use date. This sub-potent drug risk may affect the efficacy of the vasopressin injection.
Context
GovInfoNow's records show IntegraDose Compounding Services LLC has had six other recalls since Sept. 17, 2021. Recent similar recalls include an IntegraDose Vasopressin recall on May 18, 2026, and an IntegraDose Fentanyl Citrate recall on May 12, 2026. Other recent recalls of similar products include a Kirkman VasoCaine Spray recall (Feb. 18, 2026), a Baxter Vasopressin Injection recall (Aug. 6, 2026), and a Somerset Therapeutics Dexamethasone Injection recall (Feb. 4, 2026).
How to tell if you have this one
Check for lot numbers: 20230929VAS-2, 20231004VAS-2, 20231010VAS-2, or 20231013VAS-2. These syringes were compounded for medical use only and sold with specific expiration dates.
Brand
IntegraDose
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the expiration date on the syringe label. If it has expired, do not use the medication.
Where it went and when
Where it was distributed
Distributed in Minnesota.
Listed by the agency
Not listed
FDA distribution: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA published this recall 30 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-0325-2024 (January 22, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0325-2024 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.