PlainRecalls
FDA Drug Moderate Class II Terminated

Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00

Reported: October 31, 2018 Initiated: August 10, 2018 #D-0089-2019

Product Description

Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00

Reason for Recall

Incorrect Product Formulation

Details

Units Affected
80 syringes
Distribution
Nationwide
Location
Gainesville, FL

Frequently Asked Questions

What product was recalled?
Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00. Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy. Units affected: 80 syringes.
Why was this product recalled?
Incorrect Product Formulation
Which agency issued this recall?
This recall was issued by the FDA Drug on October 31, 2018. Severity: Moderate. Recall number: D-0089-2019.