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Class IIOngoing

Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride recall

FDA recall D-0258-2024 · initiated Jan 12, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Jan 31, 2024How we research

IntegraDose Compounding Services LLC recalled Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride in Jan 2024 — an FDA Class II recall (D-0258-2024) because Subpotent Drug.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Subpotent Drug

Wrong strength, or it did not keep

The product did not contain what the label promised, or stopped meeting specification before its expiry date. Under-strength medicine can mean an untreated condition.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot #: 20230921VAS-2, Exp. Date 03/19/2024

Quantity recalled: 281 syringes

Details

Product
Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-0190-1
Recalling company
IntegraDose Compounding Services LLC
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
MN only
Initiated
Jan 12, 2024
FDA report date
Jan 31, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride recalled?
IntegraDose Compounding Services LLC recalled Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride in Jan 2024 — an FDA Class II recall (D-0258-2024) because Subpotent Drug. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride recalled?
Per the FDA enforcement record, the reason for recall D-0258-2024 was: Subpotent Drug
Is a recalled Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride are affected?
Distributed: MN only. The recall covers these lots — Lot #: 20230921VAS-2, Exp. Date 03/19/2024. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0258-2024.

Source: openFDA Drug Enforcement record D-0258-2024

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