FDA Drug Recalls

Recalls / Class II

Class IID-1032-2019

Product

Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10 mL Injectable Solution 1 mg/10 mL (100 mcg per mL) NDC: 42852-802-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404

Affected lot / code info
Lot: 11/01/18 8847 80261S Exp. 3/31/2019

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
1850 syringes
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-1032-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.