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.
Incorrect blister labelling.
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.
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.
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.
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).
Look for the lot number and expiration date on the blister to determine if your product is affected.
No, this recall is for incorrect blister labeling only and does not pose a safety risk.
Check the lot number and expiration date on the blister. Affected units have specific lot numbers like GNNA2 (expires 6/12/29) or JZYZ3 (expires 11/14/29).
No action is required unless you are confused about the product's identification. Check the details to confirm if your product is affected.
We’ve drafted a message you can send Straumann to request your refund or repair — edit it as you like.
Subject: Recall Z-1671-2025 — Straumann Straumann Hello, I own a Straumann that is covered by recall Z-1671-2025 from Straumann. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
