FDA Device Intelligence
HomeTOSOH CORPORATION › AIA-PACK PAP SAMPLE DILUTING SOLUTION

AIA-PACK PAP SAMPLE DILUTING SOLUTION

TOSOH CORPORATION · Model N/A · UDI-DI 04560189211575

JFH
10
510(k) clearances
0
Adverse events
1
Recalls
9
Facilities

Recalls

DateFirmReason
2018-03-05Tosoh Bioscience IncAsfotase Alfa (Strensiq) interferes with certain Tosoh assays which potentially causes falsely increased or falsely decreased immunoassay test results, depending upon the 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 docs
Data 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.