Phadia US Inc: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Phadia US Inc in 2015. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since launch in 2003); Multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments. Software utilized in multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments.