Nobel Biocare recalls 17.5mm Multi-Unit Abutment with missing lot and expiration dates. This affects dental implants used in jaw replacements. Consumers should check product details and contact manufacturer for verification.
The product label has missing information, such as the lot number and expiration date, as well as other information.
Nobel Biocare is recalling a dental implant abutment due to missing critical information like lot numbers and expiration dates on the product label. This could lead to improper use or safety issues if the product is not properly tracked.
The product label lacks required information such as lot numbers and expiration dates. This makes it difficult to verify the product's safety and proper usage, potentially leading to improper dental implant procedures.
Dental patients who have purchased this specific abutment for jaw replacements. Patients using the product for dental implants are most at risk if the missing information causes improper use.
Check for the product name 'Nobel Biocare 17.5mm Multi-Unit Abutment, Conical Connection NP, REF 36614' with lot number #1270802. This item was sold for dental use in the upper and lower jaw.
Look for the lot number and expiration date on the product label to confirm it is not recalled.
The recall is due to missing lot and expiration dates on the label, not an immediate safety hazard. The product is safe for use if the label information is complete.
Check for the product name 'Nobel Biocare 17.5mm Multi-Unit Abutment, Conical Connection NP, REF 36614' with lot number #1270802.
The recall does not require immediate action. Check the product label for lot and expiration dates; if missing, contact Nobel Biocare for verification.
We’ve drafted a message you can send Nobel Biocare to request your refund or repair — edit it as you like.
Subject: Recall Z-2529-2018 — Nobel Biocare Nobel Biocare Hello, I own a Nobel Biocare that is covered by recall Z-2529-2018 from Nobel Biocare. 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.
