Kerr recalls Nexus Universal trial kits with incorrect bonding agent that may cause bond failures. Affected kits have specific lot numbers. Consumers should contact Kerr for details.
An issue within production process used to package trial kits let to the inclusion of the incorrect bonding agent for the kit. Use of the incorrect bonding agent may lead to increased risk of bond failures.
Kerr is recalling certain Nexus Universal trial kits due to a packaging error that included the wrong bonding agent. Using this incorrect agent may lead to dental restorations failing to bond properly.
The trial kits were packaged with the wrong bonding agent during production. This incorrect agent may cause dental restorations to fail to bond properly, leading to potential restoration failure.
Dentists and dental technicians who use the recalled Nexus Universal trial kits. Those with the specific lot numbers are most at risk.
Check the lot numbers on the kit: 7402423, 7290257, or 7451039. The product is a dental trial kit for cementing restorations.
Look for lot numbers 7402423, 7290257, or 7451039 on the kit packaging.
The trial kits were packaged with the wrong bonding agent during production, which may cause dental restorations to fail to bond properly.
Check the lot numbers: 7402423, 7290257, or 7451039.
Contact Kerr directly for instructions on how to handle the kit.
We’ve drafted a message you can send Kerr to request your refund or repair — edit it as you like.
Subject: Recall Z-1824-2020 — Kerr Kerr Hello, I own a Kerr that is covered by recall Z-1824-2020 from Kerr. 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.
