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FDA recall, , Low risk

Straumann WB Impression Post Closed Tray

The impression post closed tray contains magenta caps instead of brown.

What happened

Straumann USA LLC, of Andover, Massachusetts, recalled its WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM, because the impression caps provided in the package are magenta instead of brown. The recall began on January 6, 2026, and was added to the FDA's Enforcement Report on February 9, 2026, with distribution nationwide in the United States.

The recalled product is the WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM, which contains the impression caps that are magenta instead of brown. The company initiated the recall due to this mix up, and the FDA classified it on February 9, 2026, as noted in the weekly enforcement report dated February 18, 2026.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:

  1. A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
  2. Talk to your health care provider before you stop using it.

Is yours affected?

Match the UDI-DI and lot code listed under your product.

A UDI-DI is the device identifier printed with the barcode on the device label.

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

    UDI-DI
    • 07630031741110
    Lot code
    • VWPX4
    • VWPX6

Recall details

Company began the recall
Sold in

US Nationwide distribution.

Company
Straumann USA LLCAndover, Massachusetts
Risk

Low risk

Using it is unlikely to cause health problems.

FDA Class III recall · How risk is rated

Event ID
98265
Recall number
Z-1337-2026
Quantity recalled
561 units

All recalls from Straumann USA LLC

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Listed on Recall Canary

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 3, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)