Merz North America, Inc. recalls

5 recalls on record · latest: September 30, 2020

Official U.S. recall history for Merz North America, Inc., compiled from official government records.

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Merz North America, Inc. recalls COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

September 30, 2020 · Medical device recalls Moderate risk The Instructions for Use (IFU) updated 03/02/2020 does not match data listed in…

Merz North America, Inc. recalls Radiesse (+) Lidocaine, Injectable Implant 1.5cc, Rx only, P/N: 8063M0K1, Merz Aesthetics. Product Usage: RADIESSE is i…

May 20, 2016 · Medical device recalls Moderate risk Complaints reported of Radiesse (+) unable to be expelled from the syringe and/…

Merz North America, Inc. recalls PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA) Injectable Implant, Model No. 8044M0K5. An…

October 26, 2015 · Medical device recalls Moderate risk The expiration date encoded in the UDI barcode on the label on the product cart…

Merz North America, Inc. recalls Radiesse (+) Lidocaine Injectable Implant 1.5cc, P/N: 8063M0K1. Indicated for subdermal implantation for the correction…

October 26, 2015 · Medical device recalls Moderate risk The expiration date encoded in the UDI barcode on the label on the product cart…

Merz North America, Inc. recalls PROLARYN Injectable Implant 1.0 cc Gel, Model No. 8602M0K5. A restorable implant material to aid in surgical reconstruc…

October 26, 2015 · Medical device recalls Moderate risk The expiration date encoded in the UDI barcode on the label on the product cart…