MBi Distributing Inc.

FDA Regulatory Profile

MBi Distributing Inc. has 7 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
D-0868-2018 · Class II · May 15, 2018
Latest inspection
Jan 12, 2018 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls7Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-0868-2018Class IINausea Drops, Homeopathic Drops for Temporary Relief of Motion Sickness, Morning Sickness, and…May 15, 2018
D-0867-2018Class IITeething Drops, Homeopathic Drops for Temporary Relief of Pain Caused by Teething, 1 Fl Ounce glass…May 15, 2018
D-0872-2018Class IIArgentum Elixir Colloidal Silver, 50 PPM Homeopathic Infection Fighter, 8 fl oz. amber PET bottle…May 15, 2018
D-0870-2018Class IIStomach Calm, Calms Upset Stomach and Aids in Treatment of Simple Diarrhea, 8 fl. oz., liquid 8…May 15, 2018
D-0873-2018Class IISilver-Zinc Throat Spray, HOMEOPATHIC IMMUNE DEFENSE, 50PPM, 4oz/50 ppm/ 120ml,amber PET bottle with…May 15, 2018
D-0871-2018Class IIExpectorant Cough Syrup, Homeopathic Syrup for Temporary Relief of Cough & Bronchitis. 8 Fl Ounces…May 15, 2018
D-0869-2018Class IIIntestinal Colic Drops, Homeopathic Drops for Temporary Relief of Flatulent Colic, 1 ounce amber…May 15, 2018

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 12, 2018Lindon, UTDrugsOfficial Action Indicated (OAI)3005482889

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3005482889Lindon, UT1Jan 12, 2018

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.