JUGGERKNOT 2 — Class II medical device recall Z-0993-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-03-21, distributed in TX. For soft tissue fixation
| Recall number | Z-0993-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-06-30 |
| Classified | 2018-03-13 |
| Reported by FDA | 2018-03-21 |
| Terminated | 2018-04-13 |
| Distributed | TX |
| Quantity | 50 |
| Lot numbers | 221890 |
| Model numbers | 912050 |
Product
JUGGERKNOT 2.9MM 2 #2 MB Product Usage: For use in hip arthroplasty
Reason for recall
For soft tissue fixation
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-0993-2018. 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.