Thommen Medical recalls a dental adapter (model 3.04.090) that may deform and become difficult to remove from handpieces during use. Affected units have lot number 17415 and UDI 07640182640705.
Dental adaptor does not conform to specifications. The dental coupling of the adapter can become deformed when being inserted into the implant may make it difficult to remove the adapter from its counterpart (e.g. the handpiece).
Thommen Medical is recalling a dental adapter that may deform and become difficult to remove from handpieces during use. This could lead to complications during dental procedures if the adapter gets stuck.
The dental coupling of the adapter can deform when inserted into implants, making it difficult to remove from the handpiece. This could cause complications during dental procedures if the adapter gets stuck.
Dental professionals using the adapter for handpieces during procedures. Those with the lot number 17415 or UDI 07640182640705 are most at risk.
Check for lot number 17415 or unique device identifier (UDI) 07640182640705 on the adapter. The adapter is used to transfer implants from packaging to patients via a plug-in connection.
Look for lot number 17415 or UDI 07640182640705 on the adapter.
The dental coupling may deform when inserted into implants, making it difficult to remove from the handpiece during procedures.
Check for lot number 17415 or UDI 07640182640705. If you have these identifiers, contact Thommen Medical for guidance.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Thommen Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1390-2019 — Thommen Medical Thommen Medical Hello, I own a Thommen Medical that is covered by recall Z-1390-2019 from Thommen Medical. 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.