Voco recalls specific Ionolux dental cement capsules (REF 2115-2122) due to incorrect plunger causing delayed or incomplete curing. Affected users should contact Voco for details.
Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for Ionolux. When these capsules are activated, curing is significantly delayed and incomplete. Processing according to the instructions for use is not possible.
Voco is recalling specific Ionolux dental cement capsules (model numbers 2115-2122) because some capsules have an incorrect plunger that delays or prevents proper curing. This means the cement won't set correctly when used as intended, potentially leading to failed dental procedures.
The recalled capsules have an incorrect plunger that lacks the proper reactive component. When activated, the cement cures significantly slower and may not set completely, making it unusable for dental procedures as instructed.
Dental professionals and patients who own or use the recalled Ionolux dental cement capsules (model numbers 2115-2122) are affected. Those using the cement for dental procedures are most at risk of improper treatment.
Check the product's catalog (REF) number on the capsule, which is one of 2115, 2117, 2118, 2119, 2120, or 2122. Also look for specific lot numbers listed in the recall notice.
Identify the catalog (REF) number on the capsule (2115, 2117, 2118, 2119, 2120, or 2122) and associated lot numbers.
Due to an error in manufacturing, some capsules have an incorrect plunger that lacks the proper reactive component, causing delayed or incomplete curing.
The recall notice does not specify a remedy; contact Voco directly for guidance on next steps.
Check the catalog (REF) number on the capsule (2115, 2117, 2118, 2119, 2120, or 2122) and associated lot numbers listed in the recall notice.
We’ve drafted a message you can send Voco to request your refund or repair — edit it as you like.
Subject: Recall Z-1143-2024 — Voco Voco Hello, I own a Voco that is covered by recall Z-1143-2024 from Voco. 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.
