FDA Drug Recalls

Recalls / Class II

Class IID-1018-2019

Product

fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210-25 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404

Affected lot / code info
Lot: 01/03/19 1645 21025P Exp. 5/3/2019

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
Advanced Pharma Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
9265 Kirby Dr, N/A, Houston, Texas 77054-2520

Distribution

Quantity
180 bags
Distribution pattern
Nationwide

Timeline

Recall initiated
2019-03-13
FDA classified
2019-03-21
Posted by FDA
2019-03-27
Terminated
2020-01-14
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1018-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.