XTANT recalls nanOss 3D bone graft substitutes with incorrectly labeled 5-year shelf life. Approved shelf life is four years. Consumers should check product labels for correct expiration dates.
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
XTANT is recalling certain nanOss 3D bone graft substitutes that were incorrectly labeled with a 5-year shelf life. The product's approved shelf life is actually four years, which could lead to improper use if the product expires before it's safe to use.
The products were labeled with a 5-year shelf life, but the approved shelf life is four years. Using the product after its four-year expiration could lead to improper medical outcomes if the product degrades or loses effectiveness.
Patients who have purchased or are using the recalled nanOss 3D bone graft substitutes for medical procedures. Those with the specific model numbers and lot numbers listed in the recall are most at risk.
Check the product label for the model number (e.g., 90-300-251008) and lot number (e.g., 385486-RP25-0080). The recalled items have specific dimensions and volumes as listed in the recall notice.
Look for the model number and lot number on the product label to confirm if it's in the recall list.
The products were incorrectly labeled with a 5-year shelf life, but the approved shelf life is four years.
Check the product label for the model number and lot number to see if it's in the recall list. If it is, contact XTANT for further instructions.
The recall is for shelf life labeling, not a safety hazard. There is no risk of serious injury from improper use.
We’ve drafted a message you can send XTANT to request your refund or repair — edit it as you like.
Subject: Recall Z-1897-2026 — XTANT XTANT Hello, I own a XTANT that is covered by recall Z-1897-2026 from XTANT. 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.