Class III

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

Straumann USA LLC · January 6, 2026

Reason for Recall

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

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

561 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1337-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.