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...
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
About Implant Direct Sybron Manufacturing, LLC
Implant Direct Sybron Manufacturing, LLC has 26 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report