Straumann WB XL Anatomic Healing Abutment XC: Incorrect Blister Labeling Recall
Straumann recalls WB XL Anatomic Healing Abutment XC dental implants due to incorrect blister labeling. Affected units have specific lot numbers and expiration dates. Consumers should check their product details to determine if they are impacted.
Lower-risk recall
Incorrect blister labelling.
Contact the company
What happened, in plain English
Straumann is recalling WB XL Anatomic Healing Abutment XC dental implants because of incorrect blister labeling. This issue does not pose a safety risk but may cause confusion during product identification. Affected units have specific lot numbers and expiration dates that consumers should verify. Read more at govinfonow.com/recall/52448-straumann-wb-xl-anatomic-healing-abutment-xc-incorrect-blister-labeling.
Source Summary by GovInfoNow · govinfonow.com/recall/52448-straumann-wb-xl-anatomic-healing-abutment-xc-incorrect-blister-labeling · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1671-2025
Cite this page
“Straumann WB XL Anatomic Healing Abutment XC: Incorrect Blister Labeling Recall.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52448-straumann-wb-xl-anatomic-healing-abutment-xc-incorrect-blister-labeling. Based on FDA recall #Z-1671-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1671-2025%22&limit=1).
Why it’s dangerous
The incorrect blister labeling means the product's identification details are not accurate. This could lead to confusion when trying to verify the product's authenticity or expiration date, but it does not pose a physical safety risk.
Who’s affected
Dental patients who own or use the WB XL Anatomic Healing Abutment XC dental implants with the listed lot numbers and expiration dates are most at risk of confusion during product identification.
How to tell if you have this one
Check the product's lot number and expiration date on the blister. Affected units have specific lot numbers (e.g., GNNA2, JZYZ3) with corresponding expiration dates (e.g., 6/12/29, 11/14/29).
- Brand
Straumann- Product
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments- Category
Medical device
What to do — step by step
Check Product Details
Look for the lot number and expiration date on the blister to determine if your product is affected.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China, Netherlands, and Sweden.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 13 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to do anything with this product?
No action is required unless you are confused about the product's identification. Check the details to confirm if your product is affected.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1671-2025 (April 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1671-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.