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Recall Notice

June 22, 2020 2 min read

Chengdu Ai Qin E-commerce Co., Ltd Issues Nationwide

Recall of TTDEYE Brand Colored Contact Lenses

June 22, 2020

FOR IMMEDIATE RELEASE

N0.200, Tian Fu Fifth Street, Gaoxin District, Chengdu, China

www.ttdeye.com

On June 22, 2020, Chengdu Ai Qin E-commerce Co., Ltd initiated a nationwide recall of 1362 pairs of colored contact lenses. The relevant series of contact lenses have been found to be distributed without FDA clearance and may pose a threat to health.

The following products are being recalled:

Name of Product

Black Starshine

Diamonds Starlight

Flower Brown

Flower Grey

Radial Brown

Radial Pink

Devil Red

Brand

TTDeye

TTDeye

TTDeye

TTDeye

TTDeye

TTDeye

TTDeye

Lot Codes

B16112100

B16112203

B16112210

B16112231

B16112109

B16112110

B16112201

 

These colored contact lenses were sold through the website www.ttdeye.com and shipped directly to the customer from 08/05/2019 - 10/11/2019.

The recalled products were manufactured August 2018 and may be identified by name of the product and the date of manufacture, “2018-08”, found on the package label.  

If you have received this product, immediately cease use and contact the company via online chat at www.ttdeye.com between 9AM and 6PM (GMT+8) or contact the company via email at info@ttdeye.com (24 hours) for further information.

The company has received no complaints to date.

Chengdu Ai Qin E-commerce Co., Ltd is notifying its customers by email and is arranging for return/replacement of all recalled colored contact lenses.

Chengdu Ai Qin E-commerce Co., Ltd is voluntarily recalling these contact lenses after becoming aware of the problem. Chengdu Ai Qin E-commerce Co., Ltd has notified the FDA of this action.

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.

  • Complete and submit the report Online: fda.gov/medwatch/report.htm
  • Regular Mail or Fax: Download from fda.gov/medwatch/getforms.htmor call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

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