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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.
See this for other years:
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  • 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.
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