Class II · Moderate risk Terminated
Adenosine Injection
Reason Lack of Assurance of Sterility
Adenosine-Mono-Phosphate Injection
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
What was recalled
Adenosine-Mono-Phosphate Injection, 200 mg/ml, compounded by Olympia Pharmacy, Orlando, FL
- Recalling firm
- Lowlite Investments, Inc. D/B/A Olympia Pharmacy
- Origin
- FL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-694-2013
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.
Other Adenosine recalls
See all
Class II · Moderate risk Terminated
Adenosine Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Adenosine Injection in all strengths
Reason Lack of sterility assurance.
Class II · Moderate risk Terminated
Adenosine in 0.9% Sodium Chloride 30mL
Reason Lack of Sterility Assurance.
Class II · Moderate risk Terminated
Adenosine all strengths
Reason Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
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