Data Foundry

Drug recalls 2018

Thyroveev — Class I drug recall D-1202-2018

Terminated recall by Hellolife, reported 2018-09-19, distributed nationwide. Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not l

Recall numberD-1202-2018
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHellolife, Grand Rapids, MI, United States
Recall initiated2018-08-23
Classified2018-09-17
Reported by FDA2018-09-19
Terminated2021-01-27
DistributedNationwide (US)
Countries outside the USAU, BE, BG, BR, CA, CH, CO, CY, CZ, DK, DO, DZ, EC, EE, GB, GR, HK, HR, HU, IE, IL, IN, IT, LT, LV, MX, NL, NO, NZ, PE, PL, PT, RO, RS, RU, SA, SE, SI, SK, TR, TW
Quantity370 bottles
Reason classesmicrobial contamination, sterility
Pathogensstaphylococcus, burkholderia
NDC49726-0025-02
Lot numbersTV/030717F
Expiration dates2019-07

Product

Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02

Reason for recall

Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1202-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.