FDA Device recall Z-0074-2017
Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula
- FDA Device
- Class II
- terminated
- Published 2016-10-19
On 2016-10-19 the FDA classified a Class II recall of Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula by Banyan Medical, citing potential lack of assurance of sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0074-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-09-07 |
| Published | 2016-10-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Banyan Medical |
| Distribution | IN, TN |
Product
Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic Use- Sterile Single Use Only. Product Code 400-008
Reason
Potential lack of assurance of sterility
Identifiers
| code_info | Lot Numbers: 140310, 140806 |
|---|
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-0074-2017%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.