Zest Anchors recalls specific Locator Overdenture Implant System models due to potential small gap between implant and abutment after assembly, which may cause complications.
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
Zest Anchors is recalling certain Locator Overdenture Implant System models because the abutment may be out of specification, leading to a small gap between the implant and abutment during assembly. This gap could cause complications for patients receiving dental implants.
The abutment component may not meet specifications, causing a small gap to form between the implant and abutment when assembled. This gap could lead to complications during the dental implant procedure, such as improper fit or infection.
Patients who have received the recalled Locator Overdenture Implant System models from Zest Anchors. Dental professionals who use these implants are most at risk of complications during patient procedures.
Check for the specific product names and lot numbers listed in the recall notice: LOCATOR Overdenture Implant with 2.4mmD x 12mmL, 2.5mm Cuff (Lot L17MB); 2.4mmD x 12mmL, 4mm Cuff (Lots Ll5PB, L166F); 2.9mmD x 10mmL, 4mm Cuff (Lots L15H7, L15H9); 2.9mmD x 14mmL, 4mm Cuff (Lot USHA); and 3.4mmD x 12mmL, 4mm Cuff (Lot L17VE).
Review the product name, lot number, and UDI number to confirm if your implant system is affected by this recall.
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
The affected models include LOCATOR Overdenture Implant with 2.4mmD x 12mmL, 2.5mm Cuff (Lot L17MB); 2.4mmD x 12mmL, 4mm Cuff (Lots Ll5PB, L166F); 2.9mmD x 10mmL, 4mm Cuff (Lots L15H7, L15H9); 2.9mmD x 14mmL, 4mm Cuff (Lot USHA); and 3.4mmD x 12mmL, 4mm Cuff (Lot L17VE).
The recall does not specify a stop-use action; the hazard is low risk and may not require immediate discontinuation.
We’ve drafted a message you can send Zest Anchors to request your refund or repair — edit it as you like.
Subject: Recall Z-2425-2020 — Zest Anchors Zest Anchors Hello, I own a Zest Anchors that is covered by recall Z-2425-2020 from Zest Anchors. 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.
