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Class I: serious health riskTerminated

Hellolife Thyroveev Recall

Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife,…

Hellolife · Grand Rapids, MI

Risk level
Class I
Reported by FDA
Sep 19, 2018
Recall ID
D-1202-2018
Check your lot numberHow we source this data

Summary

Hellolife recalled Thyroveev starting Aug 23, 2018. The FDA classified it as Class I (serious health risk) and published enforcement report D-1202-2018 on Sep 19, 2018. Reason: Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia. Status: Terminated.

Why it was recalled

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

Product description

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

Lot numbers, UPCs & expiration codes

Lot: TV/030717F, exp 7/2019

Where it was sold

Nationwide USA, Algeria Australia Belgium Brazil Bulgaria Canada Colombia Croatia Cyprus Czech Republic Denmark Dominican Republic Ecuador Estonia French Polynesia Greece Guadeloupe Guam Hong Kong Hungary India Ireland Israel Italy Latvia Lithuania Martinique Mexico Monaco Netherlands New Zealand Norway Peru Poland Portugal Romania Russia Russian Federation Saudi Arabia Senegal Serbia Slovakia Slovakia (Slovak Republic) Slovenia Swaziland Sweden Switzerland Taiwan Turkey United Kingdom

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1202-2018
Classification
Class I
Status
Terminated
Recall initiated
Aug 23, 2018
FDA report date
Sep 19, 2018
Quantity
370 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Hellolife

Original FDA data

Every field from FDA enforcement report D-1202-2018, exactly as published.

Show all FDA fields
City
Grand Rapids
State
MI
Status
Terminated
Country
United States
Event ID
80893
Address
4460 44th St SE Ste C600
Code information
Lot: TV/030717F, exp 7/2019
Postal code
49512-4150
Report date
Sep 19, 2018
Product type
Drugs
Recall number
D-1202-2018
Classification
Class I
Recalling firm
Hellolife
Product quantity
370 bottles
Termination date
Jan 27, 2021
Reason for recall
Microbial Contamination of Non Sterile Products; Products contaminated with microoganisms, including but not limited to Staphylococcus saprophyticus and Burkholderia cepacia
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide USA, Algeria Australia Belgium Brazil Bulgaria Canada Colombia Croatia Cyprus Czech Republic Denmark Dominican Republic Ecuador Estonia French Polynesia Greece Guadeloupe Guam Hong Kong Hungary India Ireland Israel Italy Latvia Lithuania Martinique Mexico Monaco Netherlands New Zealand Norway Peru Poland Portugal Romania Russia Russian Federation Saudi Arabia Senegal Serbia Slovakia Slovakia (Slovak Republic) Slovenia Swaziland Sweden Switzerland Taiwan Turkey United Kingdom
Recall initiation date
Aug 23, 2018
Initial firm notification
Letter
Center classification date
Sep 17, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1202-2018, published Sep 19, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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