Bumetanide Injection Shortage: Current FDA Status

Drug Shortages low FDA · · United States

Bumetanide Injection, a cardiovascular medication, is listed as currently in shortage by the FDA, but some manufacturers report availability as of April 2026.

What this drug shortages alert tells you, and what most readers miss

This notice was issued by FDA on April 8, 2026 and geographically references United States. Its severity classification of "low" signals how the issuing agency weighs the risk of harm if no action is taken — "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to — Drug Shortages — determines the regulatory framework behind it, which shapes what remedies (refunds, replacements, recalls, evacuations) are available to affected individuals and who holds statutory responsibility for enforcement.

Most readers skim an alert like this, check whether they are personally affected, and move on. The more useful lens is to read the alert as a data point about the issuing system: how quickly FDA detected the hazard, how precise the geographic or product-identifier scope is, and whether similar alerts have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action — a single localized drug shortages advisory is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.

For decision-making, Areazine pairs each alert with the original agency URL, the full agency name, and a timestamp so you can verify the notice against the primary source before acting on it. Tags on this item (drug-shortage, fda, medication, Bumetanide) map to related alerts in the same area of risk — browsing them together gives a clearer picture than any single notice alone, because the shape of an ongoing issue only becomes visible across multiple sequential alerts.

Bumetanide Injection Shortage

What's in Shortage

The generic drug name is Bumetanide Injection, with the brand name BUMETANIDE. It is available in injection dosage form and falls under the cardiovascular therapeutic category. The shortage status is current, with the initial posting date of 01/31/2018 and last updated on 04/02/2026.

Which Manufacturers Are Affected

Fresenius Kabi USA, LLC is the manufacturer listed. Their availability status is as follows:

  • For Bumetanide, Injection, 0.25 mg/1 mL (NDC 65219-570-04): Available. Related info: Check wholesalers for inventory. Contact info: 888-386-1300.
  • For Bumetanide, Injection, 0.25 mg/1 mL (NDC 65219-572-10): Available. Related info: Check wholesalers for inventory. Contact info: 888-386-1300.

Why There's a Shortage

No specific reason for the shortage has been provided in the source data.

What Patients Should Do

If you depend on this medication, consider talking to your pharmacist about current availability or contacting the manufacturer directly for more information. Patients should always consult their healthcare provider before making any changes related to their medication.

Source

This information is attributed to the FDA Drug Shortage Database.

Source: FDA Official Notice

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Frequently Asked Questions

What is this drug shortages alert about?
Bumetanide Injection, a cardiovascular medication, is listed as currently in shortage by the FDA, but some manufacturers report availability as of April 2026.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "low" severity. No immediate action required, but stay aware.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more drug shortages alerts?
Browse all drug shortages alerts on Areazine at areazine.com/drug-shortages/ for the latest updates from FDA and other agencies.