Merz North America, Inc.: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Merz North America, Inc. in 2020. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns in diameter of calcium hydroxylapatite (CaHA), suspended in aqueous based gel carrier. Gel carrier is composed of sodium carboxymethylcellulose, sterile water for injection, and glycerin. Product is packaged in a 1.0cc syringe and packed in a sterile pouch.