Phadia US Inc: Medical Device Recalls in 2018

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Phadia US Inc in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Phadia 1000 Instrument, Article Number 12-3800-01.
ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma. To be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia 5000.
ImmunoCAP Allergen c6, Amoxicilloyl ( Article number 14-4451-016). ImmunoCAP Specific IgE is an in vitro quantitative assay for the measurement of allergen specific IgE in human serum or plasma; to be used with the instrument Phadia 250, Phadia 1000, Phadia 2500 and Phadia 5000.