FDA Device recall Z-2107-2013
SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow
- FDA Device
- Class II
- terminated
- Published 2013-09-04
On 2013-09-04 the FDA classified a Class II recall of SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow by Spinenet, citing spineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2107-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-04 |
| Published | 2013-09-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spinenet |
| Distribution | FL |
Product
SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M). Use to aspirate bone morrow.
Reason
SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
Identifiers
| code_info | Lot # 22754F16 and #25854I17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2107-2013%22
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