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Wexford Labs, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000147951

Devices
0
Registrations
FDA
FDA recalls
1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
1000147951
Address
325 Leffingwell Ave, Saint Louis, MO, 63122

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2013

    • 10 Sep 2013 Z-0358-2014 Class II Terminated Expired active ingredient was used in the manufacture of the product. Distribution: Nationwide Distribution - USA including FL, SC, TX, MO, CA, OH, OK, MA, IN, and GA.

This is an FDA establishment record without devices in deviCERTS.