PlainRecalls
FDA Devices Moderate Class II Terminated

NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024

Reported: August 22, 2018 Initiated: June 19, 2018 #Z-2822-2018

Product Description

NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024

Reason for Recall

Mislabeled hook pouch included a transport/storage label rather than the product label containing key product information such as part number, lot number, and expiration date, etc

Details

Recalling Firm
Nico Corp.
Units Affected
204 devices
Distribution
US Nationwide distribution
Location
Indianapolis, IN

Frequently Asked Questions

What product was recalled?
NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024. Recalled by Nico Corp.. Units affected: 204 devices.
Why was this product recalled?
Mislabeled hook pouch included a transport/storage label rather than the product label containing key product information such as part number, lot number, and expiration date, etc
Which agency issued this recall?
This recall was issued by the FDA Devices on August 22, 2018. Severity: Moderate. Recall number: Z-2822-2018.