Home › TOSOH CORPORATION › AIA-PACK ACTH Sample Diluting Solution
AIA-PACK ACTH Sample Diluting Solution
TOSOH CORPORATION · Model N/A · UDI-DI 04560189212541
10
510(k) clearances
33
Adverse events
6
Recalls
20
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2025-11-03 | GET TESTED INTERNATIONAL AB | Distribution without premarket approval/clearance. |
| 2018-11-30 | Tosoh Bioscience Inc | |
| 2011-12-13 | Beckman Coulter Inc. | The recall was initiated because Beckman Coulter has confirmed that the DxH Slidemaker Stainer Floor Stand shipped with Slidemaker Stainer instruments were missing vinyl caps, expo |
| 2005-04-22 | Nichols Institute Diagnostics | Performance does not meet claims in the Directional Insert concerning correlation with the IRMA ACTH assay. |
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.