Walmart Stores
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Walmart Stores is a medical device manufacturer, with 438 devices listed in FDA GUDID and FDA 510(k) (FDA Class II, Class I and Unclassified) and 1 FDA recall as of 13 Nov 2026.
- Devices
- 438
- FDA recalls
- 1
Registry facts
- Registries
- FDA GUDID 433
- FDA 510(k) 5
- Device classes
- FDA Class II 241
- FDA Class I 172
- FDA Unclassified 22
- FDA recalls
At a glance
Market reach
- United States
- FDA recalls
What Walmart Stores makes
The company produces home-use glucose monitoring systems, including test strips and meters, along with single-use blood lancets for diabetic management. It also manufactures unscented menstrual products such as tampons and pads, as well as basic insulin syringes and autoinjector needles. Additional offerings include antimicrobial skin-cover adhesive strips and a basic electric toothbrush.
The portfolio includes devices classified as Class I, Class II, and unclassified (N/U), all listed in the FDA’s Unique Device Identifier (UDI) database. The company operates under U.S. regulatory oversight, with devices authorised for commercial distribution in the United States.
Catalogue
Search and filter all 438 devicesShowing 1-50 of 438
FDA recalls
FDA recall records list 1 recall initiated by Walmart Stores, initiated on 2014-02-26. By recorded status: 1 terminated. The reasons filed fall into these groups: manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2014
- 26 Feb 2014 Z-1810-2014 Class II Terminated Fifteen pairs of prescription, safety glasses did not meet required, industrial lens thickness; nor did these glasses have the OSHA-required manufacturer markings.
Frequently asked questions
How many devices does Walmart Stores have in the registry?
The registry currently lists 438 devices for Walmart Stores. Devices recorded under merged duplicate company entries are counted once.
Which registries list Walmart Stores's devices?
Among its 50 most recently registered devices, Walmart Stores has devices listed in FDA GUDID (50 devices).
What risk classes do Walmart Stores's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Walmart Stores's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Walmart Stores?
FDA recall records list 1 recall initiated by Walmart Stores, the most recent initiated on 26 Feb 2014. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Walmart Stores in the registry?
The most recently registered devices listed for Walmart Stores include Equate 630407, Equate WAL261012V1, Equate 1 and equate 194346726707.