Z-0167-2015Class II

Prescription eyeglass safety lenses. Vision correction

Name: Z-0167-2015 Prescription eyeglass safety lenses. Vision correction
Creator: Eyemart Express Ltd
Published: 2014-09-12
License: https://open.fda.gov/license/

Eyemart Express, LLC / initiated 2014-09-12 / Terminated / root cause: manufacturing process

FDA source

Eyemart Express Ltd began a recall of Prescription eyeglass safety lenses. Vision correction on 2014-09-12. FDA classified it as Class II and gives the reason as "Prescription eyeglass safety lenses did not meet specifications". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0167-2015
Classification: Class II
Status: Terminated
Initiated: 2014-09-12
Posted: 2014-12-16
Terminated: 2015-10-09
Recalling firm: Eyemart Express, LLC
Product: Prescription eyeglass safety lenses. Vision correction
Product code: HQG Lens, Spectacle, Non-Custom (Prescription)
Reason for recall: Prescription eyeglass safety lenses did not meet specifications.
Root cause tag: manufacturing process
FDA root cause: Employee error
Action: Eyemart Express sent an Important Recall Notice dated September 12, 2014, to all affected customers. The notice identified the product, the problem, and the action to be taken by the customer. Customers were instructed to call Eyemart Express Customer Service at 1-888-DRBARNES to discuss their lens replacement options of if they have any questions.
Quantity in commerce: 76 pairs of eyeglasses
Distribution: Nationwide Distribution including AK, AL, AR, CA, LA, MD, MO, MS, MT, NC, ND, NM, OH, OK, TN, SC, TX, VA, WI, and WV.
Product codes and lots: No lot codes are applied. The recalled products contain the following model numbers: LC Elite 1.50 80mm HC, LC Elite 1.50 80mm Suntech GRY, LC Elite Poly 75mm Suntech GRY, LC Elite Poly 77mm HC, LC SFSV 1.67 Suntech3 GRY, LC SFSV 75mm Trivex STG, LC Short Elite Poly 77mm HC, LC Short Elite Poly Suntech GRY, Poly FT-28 with scratch coat, Poly LifeRX Photo FT 7x28 Brown, Poly LifeRx Photo FT-28 Gray, Poly SFSV LifeRx Photo Gray, Poly SFSV with scratch coat, SF SUMMIT ECP 167 TRN7 GY 70mm, SF SUMMIT ECP 167 TRN7 GY 75mm, SF SV 1.53 T7 GY 75mm, SF SV 70mm PHOENIX COT, SFSV 167 Clear, Transitions VI Gray D28

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0167-2015
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0167-2015	Class II	Terminated	Voluntary: Firm initiated	2014-11-12	2014-11-03

Product code HQG

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)