Prevent G Safety Winged Blood Collection Set Glide: Hub Needle May Detach During Use
Guangzhou Improve Medical Instruments recalls Prevent G Safety Winged Blood Collection Set Glide due to risk of hub needle detaching during blood draw. Affected units have serial # 102030178 and lot # 160815. No remedy specified in recall notice.
Lower-risk recall
Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
Contact the company
What happened, in plain English
Guangzhou Improve Medical Instruments is recalling their Prevent G Safety Winged Blood Collection Set Glide because the hub needle may detach while drawing blood. This could lead to blood loss or infection if the needle isn't properly secured during use. Read more at govinfonow.com/recall/72959-prevent-g-safety-winged-blood-collection-set-glide-hub-needle.
Source Summary by GovInfoNow · govinfonow.com/recall/72959-prevent-g-safety-winged-blood-collection-set-glide-hub-needle · Updated September 17, 2026 · FDA enforcement record: FDA #Z-1217-2019
Cite this page
“Prevent G Safety Winged Blood Collection Set Glide: Hub Needle May Detach During Use.” GovInfoNow, updated September 17, 2026. https://govinfonow.com/recall/72959-prevent-g-safety-winged-blood-collection-set-glide-hub-needle. Based on FDA recall #Z-1217-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1217-2019%22&limit=1).
Why it’s dangerous
The hub needle may come out when the nurse draws blood and removes the tube. This could cause blood loss or infection if the needle isn't properly secured during use. The product is designed for single-use in medical settings.
Who’s affected
Healthcare professionals who use this blood collection set during venous blood draws. Patients receiving blood draws with this product are at risk if the needle detaches.
How to tell if you have this one
Check for serial number 102030178 or lot number 160815 on the product packaging. This blood collection set is used by healthcare professionals for venous blood draws.
- Brand
Guangzhou Improve Medical Instruments- Category
Medical device
What to do — step by step
Check Product Details
Look for serial number 102030178 or lot number 160815 on the product packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of Kansas.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1217-2019 (September 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1217-2019 to see it in context.
- Plain-language summary written by qwen3:4b on September 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.