Coltene recalls HYGENIC Dental Dam Forceps (model H01262) with specific batch numbers due to pin size larger than acceptable, potentially causing improper fit with dental dam clamps.
Multiple Coltene batches of the product have a pin size larger than acceptable, which may make it difficult for the forceps to fit appropriately with dental dam clamps.
Coltene is recalling dental dam forceps model H01262 with certain batch numbers because the pin size is too large, which may make them difficult to fit properly with dental dam clamps. This could lead to improper use during dental procedures.
The forceps have a pin size larger than acceptable in certain batches, which may cause them to not fit properly with dental dam clamps. This could lead to improper placement or removal of dental dams during procedures, potentially affecting treatment effectiveness.
Dental professionals who own or use the recalled HYGENIC Dental Dam Forceps (model H01262) with specific batch numbers listed in the recall. Those most at risk are dentists and dental technicians using the forceps for dental procedures.
Check the batch number laser marked on the forceps. The recalled batches are: 1903, 1904, 1906, 1907, 1909, 1910, 1911, 1915, 1920, 1921, 1923, 1927, 1928, 1930, 1934, 1940.
Look for the batch number laser marked on the forceps; if it matches the listed numbers (1903-1940), the forceps are recalled.
If the forceps do not fit properly with dental dam clamps, return them to Coltene for replacement.
The affected batch numbers are 1903, 1904, 1906, 1907, 1909, 1910, 1911, 1915, 1920, 1921, 1923, 1927, 1928, 1930, 1934, and 1940.
No, only return the forceps if they do not fit properly with dental dam clamps.
Check the batch number on the forceps; if it matches the listed numbers and they don't fit properly with dental dam clamps, return them to Coltene.
We’ve drafted a message you can send Coltene to request your refund or repair — edit it as you like.
Subject: Recall Z-2419-2020 — Coltene Coltene Hello, I own a Coltene that is covered by recall Z-2419-2020 from Coltene. 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.
