CLASS I Drug recall · Reported 3 Sep 2014 · FDA Enforcement Report
adenosine 90 mg in 0.9% sodium chloride recalled
Central Admixture Pharmacy Services is recalling adenosine 90 mg in 0.9% sodium chloride, distributed in Michigan, Wisconsin. The recall was initiated on 28 May 2014 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1561-2014
- FDA event ID
- 68532
- Recalling firm
- Central Admixture Pharmacy Services, Livonia, MI
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 May 2014
- FDA classified
- 25 Aug 2014
- Reported
- 3 Sep 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Sterility
- Drug class
- Injectable & IV Drugs
Timeline
| 28 May 2014 | Recall initiated by company | |
| 25 Aug 2014 | Classified by FDA | +89 days |
| 3 Sep 2014 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Non Sterility; microbial contamination identified as Aspergillus species
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
adenosine 90 mg in 0.9% sodium chloride/90 mL, Rx Only, Central Admixture Pharmacy Services, Inc., Livonia, MI 48150
Where it was distributed
Michigan and Wisconsin
Questions about this recall
Why was it recalled?
Non Sterility; microbial contamination identified as Aspergillus species
Which lots are affected?
Lot# 13-920757-0-1 through Lot# 13-920757-0-5 (5 total doses) EXP 06 JUL 2014
Where was it sold?
Michigan and Wisconsin
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 68532This product is part of a recall event; the main page for the event is del Nido Cardioplegia with Lidocaine recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | del Nido Cardioplegia with Lidocaine recalled | Central Admixture Pharmacy Services | Sterility | MI, WI | |
| CLASS I | Pediatric Cardioplegia recalled by Central Admixture Pharmacy | Central Admixture Pharmacy Services | Sterility | MI, WI | |
| CLASS I | LOW Potassium Cardioplegia recalled by Central Admixture Pharmacy | Central Admixture Pharmacy Services | Sterility | MI, WI |
More recalls from Central Admixture Pharmacy Services
All 347Other Adenosine recalls
All 7| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Adenosine Injection, USP, 60mg/ (3 mg/mL) single-dose vial recalled | Teva Pharmaceuticals USA | Sterility | Nationwide |
| Drug | CLASS II | Adenosine Injection, USP, 60mg/ (3 mg/mL) single-dose vial recalled | Teva Pharmaceuticals USA | Sterility | Nationwide |
| Drug | CLASS II | Adenosine Injection in all strengths, all doses, and all packaging recalled | Pharmedium Services | Sterility | Nationwide |
| Drug | CLASS II | Adenosine in 0.9% Sodium Chloride, 90 mg recalled by Cantrell Drug | Cantrell Drug | Sterility | Nationwide |
| Drug | CLASS II | Adenosine 1mg/ml (PF) in 0.9% Sodium Chloride recalled | Pharmakon Pharmaceuticals | Sterility | Nationwide |