Nico Corp.

FDA recalling firm · 5 enforcement events · 7 product records · 2012–2021 · IN

Nico Corp. has 5 FDA enforcement events on this register (7 product records) between 2012 and 2021: 5 device; the busiest year was 2012 with 1.

0% of its events are Class I; the most common class is Class II (5). 0 events are listed as ongoing; the recalling firm's address is in IN.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
30 Apr 2021	NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. 11ga REF: NN-1001 Mvriad-LX Illumination Pack. l3ga Intended to perform resection and removal of soft tissues and fluids under direct visualization accessories to the NICO Myriad System.	Device	Class II	2	Terminated
19 Jun 2018	NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024	Device	Class II	1	Terminated
29 Jul 2015	NICO Myriad Console Model number NN-7000 The Myriad System is a surgical system specifically designed for morcellation of soft tissue. It primarily consists of a reusable console with foot pedal and a disposable handpiece. For the morcellation and removal of tissue during pelviscopic, laparoscopic, percutaneous and…	Device	Class II	1	Terminated
24 Feb 2014	Myriad handpiece Tissue morcellator	Device	Class II	1	Terminated
17 Jul 2012	13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable and re-sterilizable obturators with coordinating single patient use, disposable sheaths (three lengths available for each: 50mm, 60mm, and 75mm). The obturator and sheath are assembled in the OR…	Device	Class II	2	Terminated

By type and class

Device5

Class II5

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Nico Corp. by year initiated.

Questions and answers

How many FDA recalls has Nico Corp. had?

5 enforcement events (7 product records) on this register, 2012–2021: 5 device.

Are any Nico Corp. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Nico Corp. recalls?

5 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.