FDA Drug Recalls

Recalls / Class II

Class IID-1025-2019

Product

Glycopyrrolate 0.6 mg/3 mL (0.2 mg per mL) Injectable Solution, 3 mL Sterile single use syringe, For IV or IM use, NDC: 42852-828-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404

Affected lot / code info
Lots: 10/31/18 2288 82822S Exp. 3/30/2019; 10/18/18 8371 82822S Exp. 3/17/2019

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
140 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-1025-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.