Class II — Guangzhou Improve Medical Instruments Co., Ltd.
| Recalling firm | Guangzhou Improve Medical Instruments Co., Ltd. |
|---|---|
| Registered facility | GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Complaints about the needle is not smooth, with discoloration, a kind of gel agglomeration on the needle tip. |
| Product | 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 consists of (1) a winged needle, (2) a flexible tubing, (3) a luer adaptor. The products and evacuated blood collection tube/ syringe are used together for the collection of venous blood. |
| Quantity | 700,000 |
| Distribution | Puerto Rico |
| Initiated | 2016-10-19 |
| Classified | 2018-08-11 |
| Recall number | Z-2790-2018 |
| Initiation | Voluntary: 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-2790-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80519/
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