Paltop recalls specific dental implants due to inconsistent surface topography. Affected units may have unreliable surface texture, potentially impacting dental procedures. Contact for details.
Surface micro/nano topography on some of the implants contained within this lot may not be consistently present over the entire surface of the implant.
Paltop is recalling certain dental implants (model 6.0mm x 10mm, catalog 20-70024P) because some have inconsistent surface texture. This could affect how the implants bond with gums or teeth, leading to improper function.
The implants may have uneven surface texture due to manufacturing inconsistencies. This could lead to poor integration with surrounding tissues, potentially causing implant failure or complications during dental procedures.
Dental patients who received the specific implant model (6.0mm x 10mm, catalog 20-70024P) from Paltop. Patients with dental implants made from this batch are most at risk.
Check for the model name 'Advanced Plus Dental Implant Dia 6.0mm L10mm', catalog number 20-70024P, and lot number W0-008254. The unique identifier (UDI) is 729010869611020-70024P.
Review the implant's model, catalog number, lot number, and unique identifier to confirm if it matches the recalled items.
If your implant has the model 'Advanced Plus Dental Implant Dia 6.0mm L10mm', catalog number 20-70024P, and lot number W0-008254, it is affected.
The recall record does not specify a remedy, so contact Paltop directly for guidance.
Check the implant's model, catalog number, lot number, and unique identifier (UDI) as listed in the recall notice.
We’ve drafted a message you can send Paltop to request your refund or repair — edit it as you like.
Subject: Recall Z-0019-2020 — Paltop Paltop Hello, I own a Paltop that is covered by recall Z-0019-2020 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.
