Sekisui Diagnostics P.E.I. Inc.: Medical Device Recalls in 2016

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Sekisui Diagnostics P.E.I. Inc. in 2016. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

2016

2017

Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic Catalog Number: 506-10: R1: 1 x 10ml, R2: 2 x 10ml Catalog Number: 506-30: R1: 3 x 10ml, R2: 6 x 10ml In-Vitro quantitative measurement of Acetaminophen in serum and plasma used m the diagnosis and treatment of acetaminophen overdose toxicity.