INVISIBLU International LLC Issues Voluntary Nationwide Recall Of Continuum Labs Lgd-4033 Due To Product Containing LGD-4033 (Ligandrol), An Investigational Drug Not Approved For Use
- Company Announcement Date:
- April 05, 2016
- FDA Publish Date:
- February 04, 2019
- Product Type:
- Reason for Announcement:
- Company Name:
- INVISIBLU International LLC
- Brand Name:
Brand Name(s)Continuum Labs
- Product Description:
Product DescriptionMarketed as a dietary supplement
Invisiblu International LLC is voluntarily recalling one lot of Continuum Labs LGD-Xtreme, 3 mg to the retail and consumer level. The product has been found to contain LGD-4033 Ligandrol.
Risk Statement: The risks of using this product are unknown. Invisiblu International has not received any reports of adverse events related to this recall.
LGD-Xtreme is marketed as a dietary supplement to promote gains of lean muscle mass. The product is packaged in a dark amber plastic bottle with ninety capsules. The affected LGD-Xtreme lot numbers are 21511166 with expiration dates of 11/2018.The product can be identified by its black label with gold trim and the Continuum Labs logo. LGD-Xtreme was sold to select end consumers in the United States via the Internet, and was exported to wholesalers in Brazil.
Invisiblu International LLC is notifying its distributors and customers by this press release and e-mail, and is asking anyone in possessing of this product to stop using and discard any unused capsules.
Consumers with questions regarding this recall can contact Invisiblu International LLC by calling (954) 233-2673, extension 1, Monday through Friday, from 9 AM to 5 PM EDT, or by sending an e-mail to: email@example.com. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
- Regular Mail: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form.
- Fax: 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
INVISIBLU INTERNATIONAL LLC
(954) 233-2673 x1