Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct Sybron Manufacturing, LLC Due to Issue with design specification; oversized condition.
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¿ Angled Abutment Part Number 6050-52-60
Quantity: 205
Why Was This Recalled?
Issue with design specification; oversized condition.
Where Was This Sold?
This product was distributed to 24 states: AL, AZ, AR, CA, DE, FL, GA, KS, LA, MA, MI, MO, NE, NY, NC, OK, OR, SC, TN, TX, UT, VA, WA, WI
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