Home/Recalls/FDA-Z-1337-2026
FDA DevicesClass III

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

Published: February 18, 2026Recall ID: Z-1337-2026Category: devicesCountry: US

Reason for Recall / Hazard

The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.

Product Description & Identification

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

Additional Source Details

FieldValue
CityAndover
StateMA
Event id98265
Address 160 Minuteman Rd
Address 2N/A
Code infoArticle Number: 065.4810; UDI-DI: 07630031741110; Lot numbers: VWPX4, VWPX6;
Postal code01810-1008
Report date20260218
Product typeDevices
Product quantity561 units
Reason for recallThe mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260106
Initial firm notificationLetter
Center classification date20260209

Overview

  • Recalling FirmStraumann USA LLC
  • StatusOngoing
  • Risk LevelClass III
  • DistributionUS Nationwide distribution.
Official Agency Alert