FDA Device recall Z-2822-2018
NICO Shepherd' s Hook - Greenberg, sterile
- FDA Device
- Class II
- terminated
- Published 2018-08-22
On 2018-08-22 the FDA classified a Class II recall of NICO Shepherd' s Hook - Greenberg, sterile by Nico, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2822-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-19 |
| Published | 2018-08-22 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Nico |
| Distribution | US |
Product
NICO Shepherd' s Hook - Greenberg, sterile. An accessory to NICO s BrainPath device Part Number: NN-8024
Reason
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
Identifiers
| code_info | Lot Number: 37LG1834 Exp. Date: 11Jan 2020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2822-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.