Straumann recalls dental screwdrivers with incorrect profile that may not fit screws, risking injury during dental procedures. Affected models include SCS Screwdriver, driver, for ratchet, short, L 21mm, stainless steel (Article 046.4:01).
Tip of the screwdriver does not have the correct configuration / profile therefore the screwdriver does not properly fit the opposing screw head and cannot pick up the screws, may result in injury
Straumann is recalling dental screwdrivers that may not fit screws properly, potentially causing injury. This affects specific models sold with a particular article number. The issue is due to an incorrect screwdriver profile that prevents secure screw engagement.
The screwdriver tip has an incorrect profile that doesn't match the opposing screw head. This prevents the screwdriver from securely picking up screws, which could lead to injury if the screwdriver slips or slips during dental procedures.
Dental professionals using the recalled screwdrivers are most at risk. The recall applies to dental surgical instruments sold with the specific model and article number.
Check for the model name 'SCS Screwdriver, driver, for ratchet, short, L 21mm, stainless steel' and article number 046.401. The lot number on the package is EHG85 with part number CXV34.
Verify the model name and article number on the product packaging.
The screwdriver tip has an incorrect profile that doesn't fit the opposing screw head, which may cause injury during dental procedures.
The recall record does not specify a remedy, so check the product details to confirm if it's affected.
Look for the model name 'SCS Screwdriver, driver, for ratchet, short, L 21mm, stainless steel' and article number 046.401. The lot number on the package is EHG85 with part number CXV34.
We’ve drafted a message you can send Straumann to request your refund or repair — edit it as you like.
Subject: Recall Z-2198-2021 — Straumann Straumann Hello, I own a Straumann that is covered by recall Z-2198-2021 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.
