Class III · Low risk Ongoing
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit
Reason Failed Tablet/Capsule Specifications
Basic Reset CBD Reset 750 True Full Spectrum Cinnamon
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Marketed without an Approved NDA/ANDA
What was recalled
Basic Reset CBD Reset 750 True Full Spectrum Cinnamon, 750 mg CBD, 1 fl. oz. (30 mL) bottle, Distributed by: Basic Reset Hendersonville, TN 37075
- Recalling firm
- Basic Reset Inc.
- Origin
- TN, United States
- Initiated by
- FDA Mandated
- FDA recall number
- D-0192-2020
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Basic recalls
See all
Class III · Low risk Terminated
Avicel DG
Reason Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
Class II · Moderate risk Terminated
NAD+ Nicotinamide Adenine Dinucleotide
Reason Product found to be Sub Potent or Exceeded reconstitution time
Class II · Moderate risk Terminated
amazon basic+care
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Class II · Moderate risk Terminated
basic+care
Reason Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
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