Keystone Dental recalls Genesis Surgical Cassette Tapered Implants with extra-large white grommets that may cause dental burs to wobble, potentially leading to injury during dental procedures.
The surgical cassette contained extra-large white grommets making the 3.8 mm and 6.5mm dental burrs wobble within the grommets in the surgical cassette.
Keystone Dental is recalling Genesis Surgical Cassette Tapered Im: 3.8 mm and 6.5 mm dental burs may wobble in the surgical cassette due to extra-large white grommets. This could cause injury during dental procedures if the burs become unstable.
The surgical cassette contains extra-large white grommets that cause the 3.8 mm and 6.5 mm dental burs to wobble. This wobbling could lead to the burs becoming unstable during dental procedures, potentially causing injury to the patient.
Dentists and dental clinics using Genesis Surgical Cassette Tapered Implants with lot numbers 38177, 38330, or 38421 are affected. Patients receiving these implants during procedures using the recalled cassettes are at risk.
Check the lot numbers on the Genesis Surgical Cassette Tapered Implants: 38177, 38330, or 38421. These cassettes are intended for dental procedures after natural tooth loss or immediate implant placement.
Verify the lot numbers on the surgical cassette: 38177, 38330, or 38421.
The surgical cassette contains extra-large white grommets that cause the 3.8 mm and 6.5 mm dental burs to wobble, potentially leading to injury during dental procedures.
Lot numbers 38177, 38330, and 38421.
Check the lot numbers on the Genesis Surgical Cassette Tapered Implants. If they match 38177, 38330, or 38421, contact Keystone Dental for guidance.
We’ve drafted a message you can send Keystone Dental to request your refund or repair — edit it as you like.
Subject: Recall Z-1485-2018 — Keystone Dental Keystone Dental Hello, I own a Keystone Dental that is covered by recall Z-1485-2018 from Keystone Dental. 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.
