Remel Inc: Medical Device Recalls in 2017
Updated on March 25, 2026.
According to to data from the FDA, there were 3 medical device recalls made by Remel Inc in 2017. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic reactions.
- Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
- CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.