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Disposable High Pressure Syringe
Union Medical Shenzhen Co.,LTD. · Model SLF107 · UDI-DI 06970286900544
DXT
Prescription
1
510(k) clearances
3,315
Adverse events (146 deaths)
69
Recalls
123
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-04-24 | Bayer Medical Care, Inc. | Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock c |
| 2026-02-27 | Medline Industries, LP | Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection |
| 2026-02-27 | Medline Industries, LP | Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2024-08-30 | Merit Medical Systems, Inc. | Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier. |
| 2024-08-30 | Merit Medical Systems, Inc. | Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier. |
| 2024-08-30 | Merit Medical Systems, Inc. | Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
