Dentech recalls Rubber Dam Clamps KSK models with specific lot numbers due to possible breakage when removing parts for safety. Consumers should check their product codes and lot numbers.
Removing parts for safety reasons due to possible breakage.
Dentech is recalling certain Rubber Dam Clamps KSK models because they may break when parts are removed for safety reasons. This could lead to injury if the clamp breaks during use.
The clamps may break when parts are removed for safety reasons, potentially causing injury if the broken parts are sharp or cause cuts during dental procedures.
Dentech Rubber Dam Clamp KSK users who own the recalled models with specific product codes and lot numbers listed in the recall notice. Dental professionals and patients using these clamps during dental treatments are most at risk.
Check your product code (01012912, 01014912, 01019912, 01012913, 01014913, 01019913, 01012026, 01014026, 01019026) and lot numbers listed in the recall notice. The clamps are used for saliva and moisture prevention during dental treatments.
Identify your product code and lot number to confirm if your clamp is recalled.
Reach out to Dentech for further instructions on how to handle the recalled clamps.
The recall is due to possible breakage when parts are removed for safety reasons, which could lead to injury.
Check your product code and lot number against the list provided in the recall notice.
Contact Dentech for instructions on how to handle the recalled clamps.
We’ve drafted a message you can send Dentech to request your refund or repair — edit it as you like.
Subject: Recall Z-1676-2021 — Dentech Dentech Hello, I own a Dentech that is covered by recall Z-1676-2021 from Dentech. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
