SpineNet Bone Marrow Aspiration Needle Kit — Class II medical device recall Z-2107-2013
Terminated recall by SpineNet, reported 2013-09-04, distributed in FL. SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
| Recall number | Z-2107-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SpineNet, Winter Park, FL, United States |
| Recall initiated | 2013-02-04 |
| Classified | 2013-08-27 |
| Reported by FDA | 2013-09-04 |
| Terminated | 2013-11-15 |
| Distributed | FL |
| Quantity | 100 units |
| Lot numbers | 22754F16, 25854I17 |
Product
SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow.
Reason for recall
SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
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-2107-2013. 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.