Nobel Biocare recalls certain implant retrieval instruments due to packaging issues that could risk contamination during shelf life. Consumers should check product details and contact the company for guidance.
Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain sterile during their shelf-life.
Nobel Biocare is recalling specific implant retrieval instruments because their packaging may not keep them sterile for the full shelf life. This could lead to infections if the instruments are used without proper sterilization.
The packaging sealing process at the supplier has a problem that might not keep the instruments sterile. If the instruments become contaminated, they could cause infections during medical procedures.
Medical professionals who use these instruments for implant removal are most at risk. Patients who have received these instruments may not be directly affected unless they are using them for procedures.
Check for the product code 37472 or Tri-Chi in the packaging. These instruments are used to remove implants with specific connections.
Look for the product code 37472 or Tri-Chi on the packaging to confirm if it's affected.
The recall states that the instruments may not stay sterile, which could lead to infections if used without proper sterilization.
Check for the product code 37472 or Tri-Chi on the packaging. These instruments are used to remove implants with specific connections.
The recall does not specify a remedy, so contact Nobel Biocare for guidance.
We’ve drafted a message you can send Nobel Bioc: The brand name from the manufacturer title is to request your refund or repair — edit it as you like.
Subject: Recall Z-1317-2020 — Nobel Bioc: The brand name from the manufacturer title is Nobel Bioc: The brand name from the manuf Hello, I own a Nobel Bioc: The brand name from the manufacturer title is that is covered by recall Z-1317-2020 from Nobel Bioc: The brand name from the manufacturer title is. 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.
