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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Device
Medical Devices/Implants & Prosthetics

Straumann WB Impression Posts Recalled for Incorrect Impression Caps

Agency Publication Date: February 9, 2026
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Summary

Straumann USA LLC is recalling 561 units of the WB Impression Post Closed Tray system because the package contains the wrong impression caps. The provided caps are magenta instead of the required brown, which could lead to errors during dental procedures. This recall affects specific dental devices used for impressions of dental implants, including guide screws.

Risk

The use of an incorrectly colored impression cap may lead to an improper fit or misidentification during the dental impression process, potentially requiring the procedure to be repeated or causing fitment issues with the final dental restoration.

What You Should Do

  1. Check your inventory for WB Impression Post Closed Tray kits (L 13mm) with Article Number 065.4810 and Lot numbers VWPX4 or VWPX6.
  2. Examine the impression caps inside the package; if they are magenta instead of brown, do not use the product.
  3. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) if you have additional questions or wish to report an incident.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM
Variants: Magenta caps instead of brown
Model / REF:
065.4810
Lot Numbers:
VWPX4
VWPX6
UDI:
07630031741110

Recall Z-1337-2026; 561 units affected.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98265
Status: Active
Manufacturer: Straumann USA LLC
Sold By: authorized dental distributors; direct sales
Manufactured In: United States
Units Affected: 561 units
Distributed To: Nationwide

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.