Device Brand Name: Distal Radius Fracture Repair System Device… — Class II medical device recall Z-2212-2014
Terminated recall by Biomet, Inc., reported 2014-08-20, distributed in AL, AZ, CA, CO, GA, IA, IL, MD…. The firm received complaints indicating that the drill guide becomes stuck in the jig. The drill guide can be
| Recall number | Z-2212-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-06-23 |
| Classified | 2014-08-13 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2015-07-14 |
| Distributed | AL, AZ, CA, CO, GA, IA, IL, MD, NC, NY, PA, VA |
| Countries outside the US | AR, NL |
| Quantity | 37 |
| Lot numbers | NB0311, NB0611 |
Product
Device Brand Name: Distal Radius Fracture Repair System Device Classification Name: Plate, Fixation, Bone Device Common Name: Drill Guide DNP 3.3mm Labeling: DRILL GUIDE DNP 3.3 MM NON-STERILE LOT NB0311 QTY 1 DePuy P.O Box 988 Warsaw IN 46581
Reason for recall
The firm received complaints indicating that the drill guide becomes stuck in the jig. The drill guide can be placed in the jig about halfway before it becomes stuck.
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-2212-2014. 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.