Diasorin Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimensClass IINov 7, 2024Customer complaints were received alleging leaking devices a	Customer complaints were received alleging leaking devices and insufficient buffer volume. Diasorin's internal	Class IIDevices	Nov 7, 2024
DiaSorin LIAISON HSV-2 Type Specific IgG, REF 310620Class IIDec 13, 2023DiaSorin has identified that lots 136344, 136344A, 136344B,	DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520, 136520A, 136520B, 136520C, 136604	Class IIDevices	Dec 13, 2023