Voco recalls specific IonoStar Plus dental cement capsules (REF 2540-2549) due to incorrect plunger causing delayed or incomplete curing. Affected units may not process properly with standard instructions.
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 certain IonoStar Plus dental cement capsules because some have an incorrect plunger that causes delayed or incomplete curing. This means the cement won't set properly when used as directed, potentially leading to failed dental procedures.
The capsules contain an incorrect plunger that lacks the proper reactive component for Ionolux. When activated, this causes curing to be significantly delayed or incomplete, making the cement unusable per the manufacturer's instructions.
Dentists and dental technicians who use the recalled IonoStar Plus capsules (REF numbers 2540-2549) are affected. Those using the capsules without proper verification are at higher risk of failed dental procedures.
Check the catalog (REF) numbers on the capsule: 2540, 2543, 2544, 2545, 2546, 2547, or 2549. Also look for specific lot numbers listed in the recall notice.
Identify the catalog (REF) number on the capsule to confirm if it's in the recall list (2540, 2543, 2544, 2545, 2546, 2547, or 2549).
Due to an error in manufacturing, some capsules have an incorrect plunger that causes delayed or incomplete curing when activated.
Check the catalog (REF) number on the capsule: affected units are 2540, 2543, 2544, 2545, 2546, 2547, or 2549.
The recall does not specify a remedy, so contact Voco directly for guidance on handling affected units.
We’ve drafted a message you can send Voco to request your refund or repair — edit it as you like.
Subject: Recall Z-1142-2024 — Voco Voco Hello, I own a Voco that is covered by recall Z-1142-2024 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.
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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.
