US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 1, 2016 (10 years ago)

Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.

What was recalled

Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109

Recalling firm
Isomeric Pharmacy Solution, LLC
Origin
UT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1454-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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Class II · Moderate risk Ongoing

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Reason cGMP deviations: Temperature abuse

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