Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA LLC Due to The mix up of the impression caps provided...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Straumann USA LLC directly.
Affected Products
WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
Quantity: 561 units
Why Was This Recalled?
The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Straumann USA LLC
Straumann USA LLC has 11 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report