HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm… — Class II medical device recall Z-3261-2018
Terminated recall by Biomet UK Ltd., reported 2018-10-03, distributed nationwide. HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw n
| Recall number | Z-3261-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet UK Ltd., Bridgend, United Kingdom |
| Recall initiated | 2018-08-09 |
| Classified | 2018-09-27 |
| Reported by FDA | 2018-10-03 |
| Terminated | 2020-05-12 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Lot numbers | 3222008 |
| Model numbers | 2110-130-004 |
Product
HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-130-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
Reason for recall
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
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-3261-2018. 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.