Home › Shenzhen YHLO Biotech Co., Ltd. › iFlash-T4
iFlash-T4
Shenzhen YHLO Biotech Co., Ltd. · Model C86026 · UDI-DI 06925912718512
10
510(k) clearances
100
Adverse events
1
Recalls
13
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-04 | DRG International, Inc. | An incoming complaint reported that the expiration date on the kit box label and Certificate of Analysis (CoA) exceeded the shelf life of the standards and control solutions in the |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
