Paltop recalls specific dental implants due to incorrect screw packaging. The Standard Platform Cover Screw won't fit the Narrow Platform implant, causing potential misfit issues.
Some of the implants were packaged with a Standard Platform Cover Screw instead of a Narrow Platform Cover Screw. The Standard Platform Cover Screw will not fit in the Narrow Platform implant.
Paltop is recalling certain dental implants because some were shipped with the wrong screw type. This could cause the implant to not fit properly during installation, leading to complications.
The implants were packaged with a Standard Platform Cover Screw instead of the required Narrow Platform Cover Screw. This mismatch means the screw won't fit the implant, potentially causing installation issues or complications.
Dental professionals who purchased the specific implant model (Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020) are affected. Patients using these implants are at risk of improper fit.
Check for the product name 'Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm' and catalog number 21-70020. The recall includes items with UDI: 07290108695649 and lot number WO-011320.
Verify the product name, catalog number, and UDI to confirm if your implant is affected.
The implants were packaged with a Standard Platform Cover Screw instead of the required Narrow Platform Cover Screw, which won't fit the implant.
Check for the product name 'Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm' and catalog number 21-70020, along with UDI: 07290108695649 and lot number WO-011320.
The recall does not specify a remedy, so contact Paltop Advanced Dental Solutions Ltd for guidance.
We’ve drafted a message you can send Paltop to request your refund or repair — edit it as you like.
Subject: Recall Z-0836-2020 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0836-2020 from Paltop. 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.
