Guangzhou, N/A, China
Guangzhou Improve Medical Instruments Co., Ltd. recalls
3 recalls recorded since 2018, most recently on 22 September 2017. 3 are listed as ongoing. Status and classification are as published by the FDA.
Recalls3
Ongoing (FDA)3
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 22 September 2017
- Reason
- Leaks complaints.
- Distribution
- Kansas
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2549-2018
- Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
Ongoing Class II Medical devices
- Recall started
- 22 September 2017
- Reason
- Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
- Distribution
- US Nationwide distribution in the state of Kansas.
- Initiated
- Voluntary: Firm initiated
- Recall number
- 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, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle
Ongoing Class II Medical devices
- Recall started
- 19 October 2016
- Reason
- Complaints about the needle is not smooth, with discoloration, a kind of gel agglomeration on the needle tip.
- Distribution
- Puerto Rico
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2790-2018
- Improve Blood Collection Sets with Multiple Sample Luer Adapter - Sterile/EO Product Usage: The Blood Collection Set are single-use, sterile, winged needle bonded to a flexible tubing with luer adapter. The needle c
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.