Implant Direct Sybron recalls dental implants with incorrect cap labeling. The cap may show wrong part numbers but the main vial label is correct. Consumers should check their product details.
The cap on the vial might be labeled with the incorrect part number but the main vial label is correct.
Implant Direct Sybron recalls dental implants that have a cap labeled with an incorrect part number. This could lead to confusion during use, but the main vial label remains correct. Affected users should verify their product details to ensure safety.
The cap on the vial might show the wrong part number (4.3mmD Platform 604313U 13mmL) while the main vial label is correct. This could cause confusion during dental procedures but does not pose a direct safety risk.
Dental patients who own the recalled ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U. Those with the incorrect cap label are most at risk.
Check if the cap label says '4.3mmD Platform 604313U 13mmL' while the main vial label shows '5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U'. The product was sold with lot number 68960.
Look for the cap label stating '4.3mmD Platform 604313U 13mmL' while the main vial label shows '5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U'.
Yes, the main vial label is correct. The cap label may show an incorrect part number but this does not affect safety.
Check if the cap label says '4.3mmD Platform 604313U 13mmL' while the main vial label shows '5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U'.
No, the recall does not require returning the product. The remedy is not stated in the record.
We’ve drafted a message you can send Implant Direct to request your refund or repair — edit it as you like.
Subject: Recall Z-1917-2018 — Implant Direct Implant Direct Hello, I own a Implant Direct that is covered by recall Z-1917-2018 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.
