D-0135-2019 Class II Terminated

Recalled by Avella of Deer Valley, Inc. Store 38 — Phoenix, AZ

FDA drug recall D-0135-2019 was initiated by Avella of Deer Valley, Inc. Store 38 on October 19, 2018 and is designated Class II. Reason for recall: Lack of assurance of sterility The recall status is terminated (terminated May 6, 2021). Affected quantity: 300 bags.

Recall Details

Product Type
Drugs
Report Date
November 7, 2018
Initiation Date
October 19, 2018
Termination Date
May 6, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
300 bags

Product Description

Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

Reason for Recall

Lack of assurance of sterility

Distribution Pattern

U.S.A. nationwide.

Code Information

Lot# 138-20180409@55, Exp 11/18/2018