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Showing 41–56 of 56 results

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Brazil Seed Supplement (HandNatural) – Yellow Oleander Risk (2024)

Product recalled due to the presence of yellow oleander and its components in the product.

FDAFeb 9, 2024Nationwide• HandNatural

Brazil Seed Supplement (HandNatural) – Yellow Oleander Risk (2024)

Product recalled due to the presence of yellow oleander and its components in the product.

FDAFeb 9, 2024Nationwide• HandNatural

Brazil Seed 2-Pack (HandNatural) – Yellow Oleander Risk (2024)

Product recalled due to the presence of yellow oleander and its components in the product.

Class IHigh

FDAFeb 9, 2024Nationwide• HandNatural

Brazil Seed 2-Pack (HandNatural) – Yellow Oleander Risk (2024)

Product recalled due to the presence of yellow oleander and its components in the product.

FDAFeb 9, 2024Nationwide• HandNatural

Brazil Seed Supplement (HandNatural) – Yellow Oleander Risk (2024)

Product recalled due to the presence of yellow oleander and its components in the product.

FDAFeb 9, 2024Nationwide• HandNatural

PHENYLephrine HCl Lower Dose IV Solution (Denver Solutions) – Double Dose Risk (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

Vancomycin IV Bag (Denver Solutions) – Dosage Malfunction (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

VANCOmycin HCl IV Solution (Denver Solutions) – Double Dose Risk (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

PHENYLephrine HCl IV Solution (Denver Solutions) – Double Dose Risk (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

FentaNYL Citrate Large IV Solution (Denver Solutions) – Double Dose Risk (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

FentaNYL Citrate IV Solution (Denver Solutions) – Double Dose Risk (2023)

Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

FDADec 28, 2023Nationwide• Denver Solutions, LLC DBA Leiters Health

Reumo Flex Caplets (Botanical Be) – undeclared ingredient (2023)

Undeclared Allergen

Marketed Without an Approved NDA/ANDA: products found to contain undeclared diclofenac.

FDAOct 20, 2023Nationwide• Botanical Be

Vy&Tea Supplement (Qikmoov) – Undeclared Ingredient (2021)

Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.

FDAJul 14, 2021Nationwide• Qikmoov LLC

Green Raisin (Commerce International) – undeclared sulfites (2016)

Undeclared Allergen

Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

FDAAug 5, 2016FL• Commerce International Inc.

Green Raisin (Commerce International) – undeclared sulfites (2016)

Undeclared Allergen

Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

FDAAug 5, 2016FL, GA, NC +1 more• Commerce International Inc.

Blue Male Enhancement Pill (Menz Club) – Unapproved Ingredient (2012)

Marketed without an Approved NDA/ANDA; product found to contain sulfoaildenafil, an analogue of sildenafil, the active ingredient in a FDA approved product used for erectile dysfunction, making it an unapproved new drug

FDAMar 10, 2012UT• The Menz Club, LLC

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