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Implant Direct Sybron Manufacturing, LLC recalls REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Recalled July 11, 2018 · FDA recall Z-2376-2018 · Implant Direct Sybron Manufacturing
Hazard
Due to out of specification, the clinician would not be able to fit and engage the abutment with the implant · FDA Class II
Units
60 units
Sold at
CA, FL, GA, IL, LA, MI, MT, NC, NJ, NY, OK, OR, SC, SD, TN & WA; International: Jordan, Great Britain, Germany, Spain, Italy & Poland
Description
Due to out of specification, the clinician would not be able to fit and engage the abutment with the implant
Product
REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
Manufacturer(s)
Implant Direct Sybron Manufacturing, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →