FDA Device recall Z-0301-2021
5.5MM Arthrogarde Hip Access Cannula
- FDA Device
- Class II
- terminated
- Published 2020-11-04
On 2020-11-04 the FDA classified a Class II recall of 5.5MM Arthrogarde Hip Access Cannula by Smith And Nephew, citing the J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0301-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-09-21 |
| Published | 2020-11-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Smith And Nephew |
| Distribution | CA, CO, CT, DE, GA, IA, IL, IN, MD, MO, NC, NY, OH, PA, SC, TN, TX, WA, WI, WV |
Product
5.5MM Arthrogarde Hip Access Cannula
Reason
The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
Identifiers
| code_info | Model: 72201743, Lot: 50838788, 50834909,50846565, 50842905 & 50822169. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0301-2021%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.