Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve… — Class II medical device recall Z-3252-2018
Terminated recall by Zimmer Biomet, Inc., reported 2018-10-03, distributed in AZ, CO, FL, GA, LA, MA, MO, NY…. Expiration date incorrectly listed on the label
| Recall number | Z-3252-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2018-08-03 |
| Classified | 2018-09-26 |
| Reported by FDA | 2018-10-03 |
| Terminated | 2020-04-10 |
| Distributed | AZ, CO, FL, GA, LA, MA, MO, NY, SC, TX |
| Quantity | 217 units |
| Reason classes | labeling |
| Lot numbers | 053940, 067490, 165770, 165830, 415590, 545740, 664610, 676180, 688250, 860050 |
| Model numbers | 110016992 |
Product
Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for use in: Shoulder, Foot and Ankle, Knee, Hand and Wrist and Hip repair.Stainless Steel, Sterile Item Number: 110016992
Reason for recall
Expiration date incorrectly listed on the label
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-3252-2018. 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.