CLASS II ONGOING Drug recall · Reported 24 Jun 2026 · FDA Enforcement Report
Vasopressin in 0.9% Sodium Chloride, syringe recalled
IntegraDose Compounding Services is recalling Vasopressin in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC, distributed nationwide in the US. The recall was initiated on 18 May 2026 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0593-2026
- FDA event ID
- 99014
- Recalling firm
- IntegraDose Compounding Services, Shoreview, MN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 18 May 2026
- FDA classified
- 12 Jun 2026
- Reported
- 24 Jun 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Potency & Assay
- Drug class
- Injectable & IV Drugs
Timeline
| 18 May 2026 | Recall initiated by company | |
| 12 Jun 2026 | Classified by FDA | +25 days |
| 24 Jun 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Subpotent Drug
Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.
Product as listed by the FDA
Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N, Suite 900, Shoreview, MN, NDC 71139-0190-1.
Where it was distributed
U.S.A. Nationwide
Questions about this recall
Why was it recalled?
Subpotent Drug
Which lots are affected?
Lot#: 20260327VAS-3, BUD: 05/26/2026; 20260320VAS-3, BUD: 05/19/2026.
Where was it sold?
U.S.A. Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.