FDA Device recall Z-1217-2019
Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood Collection Set is single-use,…
- FDA Device
- Class II
- ongoing
- Published 2019-05-01
On 2019-05-01 the FDA classified a Class II recall of Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood Collection Set is single-use,… by Guangzhou Improve Medical Instruments, citing complain due to the hub needle came out when the nurse draw the blood and removed the tube.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1217-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-09-22 |
| Published | 2019-05-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Guangzhou Improve Medical Instruments |
| Distribution | US |
Product
Prevent G Safety Winged Blood Collection Set Glide - Rx Only -Sterile/EO - Product Usage: The IMPROSAFE Blood Collection Set is single-use, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle consists of (1) a winged needle, (2) a flexible tubing, (3) a luer adaptor. (4) a safety shield, The products and evacuated blood collection tube/ syringe are used together for the collection of venous blood.
Reason
Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
Identifiers
| code_info | Serial # 102030178 / Lot # 160815 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1217-2019%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.