Nico recalls

Nico has 7 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 16 Jun 2021. The most frequent reason is labeling errors.

Total recalls7since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 16 Jun 2021

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 7 100%Class III 0 0%

Why nico is recalled

Product types

Other Medical Devices571%
Surgical Instruments229%

By year

2021229%
2018114%
2016114%
2015114%
2012229%

All nico recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
16 Jun 2021Device	CLASS II	Myriad-LX Illumination Pack recalled by Nico	Nico	Other	Nationwide
16 Jun 2021Device	CLASS II	Myriad-LX Light Source-for delivery of light to recalled by Nico	Nico	Other	Nationwide
22 Aug 2018Device	CLASS II	Shepherd' s Hook - Greenberg, sterile recalled by Nico	Nico	Labeling Errors	Nationwide
29 Jun 2016Device	CLASS II	Myriad handpiece Tissue morcellator recalled by Nico	Nico	Device Malfunction	13 states
23 Sep 2015Device	CLASS II	Myriad Console recalled by Nico	Nico	Device Malfunction	4 states
22 Aug 2012Device	CLASS II	BrainPath Sheath The NICO BrainPath is a family of products recalled	Nico	Labeling Errors	MI
22 Aug 2012Device	CLASS II	BrainPath Sheath The NICO BrainPath is a family of products recalled	Nico	Labeling Errors	MI

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.