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Straumann WB Impression Post Closed Tray
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MEDICAL DEVICE RECALLLOW

Straumann WB Impression Post Closed Tray

Straumann is recalling WB Impression Post Closed Tray kits (L 13mm) due to incorrect magenta impression caps instead of brown.

What to do

Stop using the affected WB Impression Post Closed Tray kits immediately. Contact Straumann USA LLC to verify whether your kit is affected and to obtain the correct brown impression caps or a replacement kit.

Recalled
Listed
Updated
Recall No.
Z-1337-2026
Agency
FDA
Firm
Straumann USA LLC
Recall ID
98265
Status
ONGOING

Recall at a glance

Quantity recalled
561 units

Why it was recalled

Straumann USA LLC is recalling WB Impression Post Closed Tray kits (L 13mm, TAN/POM) distributed nationwide due to incorrect impression caps included in the package. The kits contain magenta impression caps instead of the specified brown caps, which may result in using the wrong component for the intended procedure.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

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

UDI-DI
07630031741110

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other recent recalls from Straumann USA LLC

All recalls from Straumann USA LLC

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Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification