CLASS II ONGOING Device recall · Reported 1 Aug 2018 · FDA Enforcement Report
Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO recalled
Guangzhou Improve Medical Instruments Co is recalling Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO, distributed in Kansas. The recall was initiated on 22 Sep 2017 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2549-2018
- FDA event ID
- 80524
- Recalling firm
- Guangzhou Improve Medical Instruments Co, Guangzhou, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 22 Sep 2017
- FDA classified
- 26 Jul 2018
- Reported
- 1 Aug 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Sterility
- Device type
- Syringes & Needles
Timeline
| 22 Sep 2017 | Recall initiated by company | |
| 26 Jul 2018 | Classified by FDA | +307 days |
| 1 Aug 2018 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Leaks complaints.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
Where it was distributed
Kansas
Questions about this recall
Is Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO recalled?
Yes. Guangzhou Improve Medical Instruments Co recalled Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO on 22 Sep 2017. The recall is Class II and its status is Ongoing. Recall number Z-2549-2018.
Why was it recalled?
Leaks complaints.
Which lots are affected?
Serial Number 102030178 Lots #: 160809
Where was it sold?
Kansas
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Guangzhou Improve Medical Instruments Co
All 3| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Prevent G Safety Winged Blood Collection Set Glide recalled | Guangzhou Improve Medical Instruments Co | Sterility | Nationwide |
| Device | CLASS II | Improve Blood Collection Sets recalled by Guangzhou Improve Medical | Guangzhou Improve Medical Instruments Co | Sterility | PR |
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