FDA Device recall Z-0690-2016
Lipogems SPA Aspiration Cannulae, intended for aspiration of adipose tissue
- FDA Device
- Class II
- terminated
- Published 2016-02-03
On 2016-02-03 the FDA classified a Class II recall of Lipogems SPA Aspiration Cannulae, intended for aspiration of adipose tissue by Globalmed Logistix, citing the cannulae may bend during procedure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0690-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-12-15 |
| Published | 2016-02-03 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Globalmed Logistix |
| Distribution | CA, CO, CT, FL, GA, NJ, NY |
Product
Lipogems SPA Aspiration Cannulae, intended for aspiration of adipose tissue. LGC 13G (13G x 185mm), Sterile.
Reason
The cannulae may bend during procedure.
Identifiers
| code_info | Ref # AR1318, Lot AB 0643 and AB 0732. Expiration date 04/2020. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0690-2016%22
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