ImplantDirect Legacy 2 dental implants (4.7mmD x 11.5mmL) may have incorrect size labeled on packaging. Consumers should check product details and contact manufacturer for verification.
Packaged dental implant contains a different size then the size declared on the labeling.
ImplantDirect is recalling Legacy 2 dental implants that may have a different size than what's labeled on the packaging. This mismatch could lead to improper fitting during dental procedures, potentially causing complications.
The dental implant packaging may list a different size than the actual implant. This discrepancy could cause improper fitting during dental procedures, potentially leading to complications like incorrect placement or surgical issues.
Dental patients who purchased Legacy 2 implants from ImplantDirect. Patients using these implants for dental procedures are most at risk if the size mismatch affects surgical planning.
Check for the product name 'Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform' on the packaging. Look for lot number 166297 or unique device identifier (UDI) 10841307101789.
Verify the product name and lot number on the packaging to confirm if it matches the recalled items.
The packaging may list a different size than the actual implant, which could lead to improper fitting during dental procedures.
Check for the product name 'Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform' and lot number 166297 or UDI 10841307101789 on the packaging.
No immediate action is required. Check the product details to confirm if it matches the recalled items.
We’ve drafted a message you can send Implant Direct to request your refund or repair — edit it as you like.
Subject: Recall Z-0197-2022 — Implant Direct Implant Direct Hello, I own a Implant Direct that is covered by recall Z-0197-2022 from Implant Direct. 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.
