Lipotropic (l-carnitine + Methylcobalamin + Thiamine + recalls

The FDA has published 1 recall involving Lipotropic (l-carnitine + Methylcobalamin + Thiamine + since 2017. The latest was reported on 11 Jan 2017. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2017
Last 12 months0reported
Class I00% of total
Ongoing1latest 11 Jan 2017

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why lipotropic (l-carnitine + methylcobalamin + thiamine + is recalled

Companies

By year

Ongoing lipotropic (l-carnitine + methylcobalamin + thiamine + recalls

1 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILipotropic (L-Carnitine 170 mg + Methylcobalamin 300 mcg + recalledTri-Coast PharmacySterilityNationwide

All lipotropic (l-carnitine + methylcobalamin + thiamine + recalls, newest first

1 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILipotropic (L-Carnitine 170 mg + Methylcobalamin 300 mcg + recalledTri-Coast PharmacySterilityNationwide

Should you stop taking Lipotropic (l-carnitine + Methylcobalamin + Thiamine +?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.