Reported Mar 11, 2020 · Terminated

BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML]…

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical · 1990 Westwood Blvd Ste 135 · Los Angeles, CA · 90025-4650

Is this the product you have?

  • BETAMETHASONE ACETATE/BETAMETHASONE (PF) Injectable Suspension, Betamethasone Acetate/Betamethasone (PF) CMC [2ML] 6MG/ML INJ SUSP, For IM, IA, IT Use, Shake Well. Preservative Free. Discard Unused Portion, 2 mL Single-use Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0620-2
Lot codes and dates
    • Lot #: 10022019+53004
    • Exp 2/28/2020
    • 11252019+53282
    • Exp 6/12/2020
Amount recalled
N/A

This recall covers 63 products

The agency filed one notice per product. You are reading one of them; the other 62 are below.

50 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Lack of Assurance of Sterility

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Dec 7, 2023 · Data as of Sep 19, 6:39 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.