FDA Device recall Z-0993-2018
JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty
- FDA Device
- Class II
- terminated
- Published 2018-03-21
On 2018-03-21 the FDA classified a Class II recall of JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty by Zimmer Biomet, citing for soft tissue fixation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0993-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-30 |
| Published | 2018-03-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | TX |
Product
JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty
Reason
For soft tissue fixation
Identifiers
| code_info | Part number: 912050 Lot number: 221890 |
|---|
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-0993-2018%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.