Merz North America recalls

Merz North America appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2020-11-25.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns in diameter of calc…
  FDA Device · Class II · 2020-11-25 · Merz North America
• Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics
  FDA Device · Class II · 2016-08-31 · Merz North America
• PROLARYN Injectable Implant 1.0 cc Gel, Model No. 8602M0K5. A restorable implant material to aid in surgical reconstructions as a space occ…
  FDA Device · Class II · 2015-12-09 · Merz North America
• Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction of moderate to seve…
  FDA Device · Class II · 2015-12-09 · Merz North America
• PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA) Injectable Implant, Model No. 8044M0K5. An injectable implant u…
  FDA Device · Class II · 2015-12-09 · Merz North America