Neocis recalls Gen 2 Anterior Chairside Splint LLUR (DRW-0742-01) due to potential mislabeling. This may cause confusion in dental implant procedures. Affected units were sold with work order 1623.
The LRUL and LLUR posterior chairside splints and LLUR anterior chairside splints may be mislabeled.
Neocis is recalling its Gen 2 Anterior Chairside Splint LLUR (model DRW-0742-01) because it may be mislabeled. This could lead to confusion during dental implant surgery planning or procedures.
The splint may be mislabeled, which could cause confusion during dental implant surgery. This might lead to incorrect usage or procedures if the wrong splint is used.
Dental professionals who use this splint for implant surgery planning or procedures are most at risk. Affected units were sold with work order 1623.
Check for the model number DRW-0742-01 on the product. Affected units were sold with work order 1623.
Look for the model number DRW-0742-01 and work order 1623 on the product.
The splint may be mislabeled, which could cause confusion during dental implant surgery procedures.
Check the product label for model DRW-0742-01 and work order 1623. No action is needed if it's correctly labeled.
The recall is due to potential mislabeling, not a direct safety hazard. No injuries have been reported.
We’ve drafted a message you can send Neocis to request your refund or repair — edit it as you like.
Subject: Recall Z-2639-2020 — Neocis Neocis Hello, I own a Neocis that is covered by recall Z-2639-2020 from Neocis. 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.
