Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin) Recalled by Remel Inc Due to Use of affected lots may give false indication...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Remel Inc directly.
Affected Products
Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England Product is used in the semi-quantitative agar diffusion test method for in-vitro susceptibility testing.
Quantity: 60 packs
Why Was This Recalled?
Use of affected lots may give false indication of susceptibility to Nitrofurantoin.
Where Was This Sold?
This product was distributed to 17 states: AL, AR, CA, FL, GA, IL, KS, LA, MD, MA, NY, OK, PA, RI, TX, VA, WA
About Remel Inc
Remel Inc has 70 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report