FDA Device recall Z-2549-2018
Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
- FDA Device
- Class II
- ongoing
- Published 2018-08-01
On 2018-08-01 the FDA classified a Class II recall of Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO by Guangzhou Improve Medical Instruments, citing leaks complaints.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2549-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-09-22 |
| Published | 2018-08-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Guangzhou Improve Medical Instruments |
| Distribution | KS |
Product
Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
Reason
Leaks complaints.
Identifiers
| code_info | Serial Number 102030178 Lots #: 160809 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2549-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.