Torque Limiting Handle — Class II medical device recall Z-1466-2015
Terminated recall by Biomet Spine, LLC, reported 2015-04-29, distributed nationwide. Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque Limiting Handle (Aspen/ Alpine) due
| Recall number | Z-1466-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet Spine, LLC, Broomfield, CO, United States |
| Recall initiated | 2015-03-12 |
| Classified | 2015-04-20 |
| Reported by FDA | 2015-04-29 |
| Terminated | 2015-09-16 |
| Distributed | Nationwide (US) |
| Quantity | 874 |
| Model numbers | 2009300344, 2009300543, 2009300544, 2009300643, 2009300644, 2009300743, 2009300744, 2009300843, 2009300844, 2009300993, 2009411328, 2009411377, 2010082160, 2010082257, 2010152507, 2010152571, 2010373025, 2010373174, 6200-1109 |
Product
Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provides posterior fixation in the non-cervical spine with an interspinous fixation device.
Reason for recall
Biomet is recalling the Lineum HF Torque Handle Limit (Lineum) and Torque Limiting Handle (Aspen/ Alpine) due to the supplier withdrawing it from the market for component updates or reconfiguration.
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-1466-2015. 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.