WB Impression Post Closed Tray incl. guide screw recall (Straumann USA LLC)
Medical deviceClass IIIOngoing
Summary: Straumann USA LLC is recalling WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM. Reason: The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
What is being recalled
WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
Why
The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
How serious is it
Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.
Where it was sold
US Nationwide distribution.
How to tell if yours is affected
Article Number: 065.4810; UDI-DI: 07630031741110; Lot numbers: VWPX4, VWPX6;
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1337-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class III |
| Status | Ongoing |
| Recall started | January 6, 2026 |
| Reported | February 18, 2026 |
| Company | Straumann USA LLC |
| Company location | Andover, MA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 561 units |
More recalls from Straumann USA LLC · all medical device recalls · recalls from January 2026