Home / Recalls / Medical Devices
Implant Direct Sybron Manufacturing, LLC recalls RePlant¿ Angled Abutment Part Number 6050-52-60
Recalled August 10, 2016 · FDA recall Z-2320-2016 · Implant Direct Sybron Manufacturing
Hazard
Issue with design specification; oversized condition. · FDA Class II
Units
205
Sold at
U.S. distribution to the following; CA, WA, UT, GA, AZ, NE, OR, MI, TX, WI, FL, AL, AR, MO, VA, MA, TN, LA, NC, KS, NY, SC, OK. Foreign distribution to the following; CA, DE, IT, GB, PL, DE, GB, NL, GR, ES, HR, BG.
Description
Issue with design specification; oversized condition.
Product
RePlant¿ Angled 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 →