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Recall

Class II — Guangzhou Improve Medical Instruments Co., Ltd.

Recalling firmGuangzhou Improve Medical Instruments Co., Ltd.
Registered facilityGUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD. (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonComplain due to the hub needle came out when the nurse draw the blood and removed the tube.
ProductPrevent 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.
Quantity550,000
DistributionUS Nationwide distribution in the state of Kansas.
Initiated2017-09-22
Classified2019-04-24
Recall numberZ-1217-2019
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Guangzhou Improve Medical Instruments Co., Ltd. (Z-1217-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80547/

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