Clark Laboratories, Inc.: Medical Device Recalls in 2021

According to to data from the FDA, there were 2 medical device recalls made by Clark Laboratories, Inc. in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

• Bartels Legionella Urinary Antigen- an adjunct to culture for the presumptive diagnosis of past or current Legionnaire's Disease by qualitative detection of Legionella Pneumophila seragroup 1 antigen in human urine. Product Code: B1029-440
• Trinity Biotech Captia Measles IgM Kit, Catalog No. 2326060 - Product Usage: intended for the qualitative detection of Measles igM antibodies in human serum of patients suspected of measles (rubeola) infection.