Homeocare Laboratories recalls

Homeocare Laboratories has 12 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 24 Jul 2024. The most frequent reason is manufacturing (cgmp) deviations.

Total recalls12since 2023
Last 12 months0reported
Class I00% of total
Ongoing0latest 24 Jul 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 12 100%Class III 0 0%

Why homeocare laboratories is recalled

Product types

By year

All homeocare laboratories recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIStellalife Advanced Formula Peppermint, Vega Oral Care, Rinse recalledStellalife Vega Oral Care PeppermintHomeocare LaboratoriesSterilityNationwide
DrugCLASS IIKanjo Homeopathic Pain Relief Cream With Arnica recalledHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIStellaLife VEGA Oral Care Gel tubes recalled by Homeocare LaboratoriesHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIDoloEar Earache Drops recalled by Homeocare LaboratoriesHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIStellaLife VEGA Oral Care Rinse, Peppermint recalledStellalife Vega Oral Care RinseHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIStellaLife VEGA Oral Care Spray recalled by Homeocare LaboratoriesHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIBebelyn Colic Drops Homeopathic Remedy recalledHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIStellaLife VEGA Oral Care Gel tubes, Peppermint recalledStellalife Vega Oral CareHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIBabelyn Diarrhea Drops Homeopathic Remedy recalledHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide
DrugCLASS IISnoreStop Naso Spray Bulk, liquid recalled by Homeocare LaboratoriesHomeocare LaboratoriesManufacturing (CGMP) DeviationsNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.