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Nico Corp.

Complete recall history across all FDA and CPSC categories — 7 total recalls

Nico Corp. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (7)

FDA medical device enforcement actions by Nico Corp.

Date Product Reason Class
Apr 30, 2021 NICO Myriad-LX Illumination Pack: REF: NN-1000 Mvriad-LX Illumination Pack. ... (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact betw... Class II
Apr 30, 2021 Myriad-LX Light Source-for delivery of light to the surgical field to enhance... (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact betw... Class II
Jun 19, 2018 NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath ... Mislabeled hook pouch included a transport/storage label rather than the pro... Class II
Jul 29, 2015 NICO Myriad Console Model number NN-7000 The Myriad System is a surgical... Two cables within the console were inadvertently twisted during manufacturing... Class II
Feb 24, 2014 Myriad handpiece Tissue morcellator This recall has been initiated due to a defective component within the handpi... Class II
Jul 17, 2012 13.5 mm x 50 mm BrainPath Sheath The NICO BrainPath is a family of product... BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled a... Class II
Jul 17, 2012 13.5 mm x 60 mm BrainPath Sheath The NICO BrainPath is a family of product... BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled a... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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