NICO Shepherd' s Hook — Class II medical device recall Z-2822-2018
Terminated recall by Nico Corp., reported 2018-08-22, distributed nationwide. Mislabeled hook pouch included a transport/storage label rather than the product label containing key product
| Recall number | Z-2822-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nico Corp., Indianapolis, IN, United States |
| Recall initiated | 2018-06-19 |
| Classified | 2018-08-14 |
| Reported by FDA | 2018-08-22 |
| Terminated | 2018-11-09 |
| Distributed | Nationwide (US) |
| Quantity | 204 devices |
| Reason classes | labeling |
| Lot numbers | 37LG1834 |
| Model numbers | NN-8024 |
| Expiration dates | 2020-01-11 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2822-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.