Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1337-2026 — WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

U.S. FDA — Device Enforcement · United States · 2026-01-06 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1337-2026
Date of alert
2026-01-06
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Straumann USA LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07630031741110
Reported risk: The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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