Prevent G Safety Winged Blood Collection Set Glide — Class II medical device recall Z-1217-2019
Ongoing recall by Guangzhou Improve Medical Instruments Co., Ltd., reported 2019-05-01, distributed nationwide. Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
| Recall number | Z-1217-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Guangzhou Improve Medical Instruments Co., Ltd., Guangzhou, N/A, China |
| Recall initiated | 2017-09-22 |
| Classified | 2019-04-24 |
| Reported by FDA | 2019-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 550,000 |
| Lot numbers | 160815 |
| Serial numbers | 102030178 |
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 for recall
Complain due to the hub needle came out when the nurse draw the blood and removed the tube.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1217-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.