FDA Medical Device Recalls (openFDA)
Wal Mart Stores, Inc: Safety glasses made with "Rage" frames manufactured between February 20, 2014 and February 25, 2014. The color of the frames of the recalled glasses were either white or black. Safety Eye wear
- Recall number
- Z-1810-2014
- Recalling firm
- Wal Mart Stores, Inc
- Product
- Safety glasses made with "Rage" frames manufactured between February 20, 2014 and February 25, 2014. The color of the frames of the recalled glasses were either white or black. Safety Eye wear
- Status
- Terminated
- Initiated
- 2014-02-26
- Posted
- 2014-06-17
- Terminated
- 2015-01-08
- Reason
- Fifteen pairs of prescription, safety glasses did not meet required, industrial lens thickness; nor did these glasses have the OSHA-required manufacturer markings.
- Root cause
- Employee error
- Action
- Wal-Mart sent an Urgent Medical Device Recall letter dated March 12, 2014, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Actions to be taken by the Customer/User: Do not use the eyewear in any situation where safety-impact lenses are required. Replacement eyewear has been manufactured and available for the patient to pick up at the vision center where the original eyewear was purchased. Type of Action by the Company: Walmart contacted all patients on February 27 and 28. Patients were notified that their eyewear was not made at safety thickness, and that the patient should not wear the eyewear in an environment where safety thickness lenses are needed. Walmart manufactured replacement orders for all affected patients. Should you have any questions regarding this notice please call (479)277-0720
- Quantity
- 15 safety glasses
- Distribution
- US Distribution including the states of AR, AL, CA, FL, KS, LA, MN, NJ, NV,OH, TX, and SC.
- Lot, serial or model codes
- Serial Numbers: 00174-1030010, 01839-1257619, 01249-1 013988, 00036-1175608, 01052-1100006, 00359-1150914, 03283-1 055954, 00773-1 043248, 05385-1 051400, 00644-1151291, 02402-1 028575, 01903-1041038, 02294-1 024246, 03729-1 020577, 02937-1071566
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HQG
- Firm FEI
- 2316750
- Firm city
- Bentonville
- Firm state
- AR
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28