Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy 4139 Cadill
Summary
The FDA issued a Class II for Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, R by New Vitalis Pharmacy LLC dba New Vitalis Pharmacy. Reason: Lack of Assurance of Sterility.
Details
Source
Drug Recall
External ID
D-0899-2021
Action Date
2021-10-06
Status
Terminated
Category
drug
Product Description
Testosterone Cypionate Testosterone Propionate, 180mg/mL, 20mg/mL, 1 mL vial, Rx only, New Vitalis Pharmacy 4139 Cadillac Ct # 201 Louisville, KY 40213
Lot/Code Info: Lot, expiry: Lot #AL07202021@901, Exp 9/18/21; Lot #AL07272021@901, Exp 9/25/21; Lot #AL08032021@901, Exp 10/2/21; Lot #AL08102021@901, Exp 10/9/21; Lot #AL08172021@901, Exp 10/16/21; Lot #AL08242021@901, Exp 10/23/21
Quantity Affected: 1,347 vials
Reason for Recall
Lack of Assurance of Sterility
Distribution
Nationwide within the United States
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-22
Company
Louisville, KY
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 107 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (New Vitalis Pharmacy LLC dba New Vitalis Pharmacy) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does New Vitalis Pharmacy LLC dba New Vitalis Pharmacy have FDA actions?
New Vitalis Pharmacy LLC dba New Vitalis Pharmacy has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0899-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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