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.
Reported: September 4, 2013 Initiated: March 25, 2013 #Z-2081-2013
Product Description
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.
Reason for Recall
Use of affected lots may give false indication of susceptibility to Nitrofurantoin.
Details
- Recalling Firm
- Remel Inc
- Units Affected
- 60 packs
- Distribution
- US Distribution including the states of AL, AR, CA, FL, GA, IL, KS, LA, MA, MD, NY, OK, PA, RI, TX, VA, and WA.
- Location
- Lenexa, KS
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Remel Inc. Units affected: 60 packs.
Why was this product recalled? ▼
Use of affected lots may give false indication of susceptibility to Nitrofurantoin.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 4, 2013. Severity: Low. Recall number: Z-2081-2013.
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