Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

REPLANT 5.0mmD ABUTMENT Recalled by Implant Direct Sybron Manufacturing, LLC Due to Due to out of specification, the clinician would...

Date: May 18, 2018
Company: Implant Direct Sybron Manufacturing, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Implant Direct Sybron Manufacturing, LLC directly.

Affected Products

REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60

Quantity: 60 units

Why Was This Recalled?

Due to out of specification, the clinician would not be able to fit and engage the abutment with the implant

Where Was This Sold?

This product was distributed to 16 states: CA, FL, GA, IL, LA, MI, MT, NJ, NY, NC, OK, OR, SC, SD, TN, WA

Affected (16 states)Not affected

About Implant Direct Sybron Manufacturing, LLC

Implant Direct Sybron Manufacturing, LLC has 26 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report