Merz North America recalls

Merz North America has 5 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 25 Nov 2020. 1 is still ongoing.

Total recalls5since 2015

Last 12 months0reported

Class I00% of total

Ongoing1latest 25 Nov 2020

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why merz north america is recalled

Other Reasons480%
Device Malfunction120%

Product types

By year

2020120%
2016120%
2015360%

Ongoing merz north america recalls

1 active

Reported	Class	Recall	Company	Reason	Where
25 Nov 2020Device	CLASS II	Coaptite Injectable Implant, injectable, sterile recalled	Merz North America	Device Malfunction	48 states

All merz north america recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
25 Nov 2020Device	CLASS II	Coaptite Injectable Implant, injectable, sterile recalled	Merz North America	Device Malfunction	48 states
31 Aug 2016Device	CLASS II	Radiesse (+) Lidocaine, Injectable Implant 1.5cc recalled	Merz North America	Other	Nationwide
9 Dec 2015Device	CLASS II	Prolaryn Injectable Implant 1.0 cc Gel recalled by Merz North America	Merz North America	Other	Nationwide
9 Dec 2015Device	CLASS II	Radiesse (+) Lidocaine Injectable Implant 1.5cc recalled	Merz North America	Other	Nationwide
9 Dec 2015Device	CLASS II	Prolaryn Plus Injectable Implant 1.0 cc Plus Calcium recalled	Merz North America	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.