Class II · Moderate risk Terminated
Adenosine Injection
Reason Lack of Assurance of Sterility
Adenosine Injection in all strengths
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of sterility assurance.
What was recalled
Adenosine Injection in all strengths, all doses, and all packaging.
- Recalling firm
- Pharmedium Services, LLC
- Origin
- IL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0443-2018
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 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.
Class II · Moderate risk Terminated
Adenosine 1mg/ml
Reason Lack of Assurance of Sterility
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