Walmart Stores

FDA Regulatory Profile

Walmart Stores appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 5 510(k) clearances, 8 FDA inspections, and 4 compliance actions on record. Its most recent recall (D-0725-2022, Class I) was initiated on February 9, 2022. Its most recent 510(k) clearance was granted on October 25, 1995.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
5
Inspections
8
Compliance Actions
4

Known Names

walmart stores, wal-mart stores, wal-mart stores distribution center #06048, wal-mart stores, inc, wal-mart stores,inc

Recent Recalls

NumberClassProductDate
D-0725-2022Class IAvaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*, packaged in 10 Capsules per carton.February 9, 2022

Recent 510(k) Clearances

K-NumberDeviceDate
K954639SUNGLASSESOctober 25, 1995
K945819SUNGLASSESJanuary 5, 1995
K945818SUNGLASSESJanuary 5, 1995
K945817SUNGLASSESJanuary 5, 1995
K941680SUNGLASSESMay 9, 1994