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Recall

Updated: February 23, 2024 8:01 PM

H&Natural Brand Products - recalled due to Yellow oleander, USA

2 months ago •source www.fda.gov

Recall notice

San Luis, AZ, G.A. Mart dba H&Natural, is voluntarily recalling 2 lots of H&NATURAL TejoRoot, 10g pills, and 2 lots of H&NATURAL Brazil Seed, .167g Seeds to the consumer level. The products have been found via random FDA testing to contain yellow oleander, a poisonous plant native … See More

#amazon #walmart #dietarysupplements #recall #us

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Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage, USA

2 months ago •source www.fda.gov

Recall notice

Nordic Naturals is voluntarily recalling one lot of Nordic Naturals Baby’s Vitamin D3 Liquid. This recall is being conducted due to a manufacturing error that resulted in an elevated level of Vitamin D3 dosage or super potent dose. There have been no reports of adverse events to … See More

#dietarysupplements #recall #us

Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage photo #1

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Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil, USA

3 months ago •source www.fda.gov

Recall notice

“Today The World” is voluntarily recalling two lots of Sustain herbal dietary supplement capsules and one lot of Schwinnng capsules to the consumer level. FDA analysis has found the products to contain undeclared Tadalafil and Nortadalafil. Products were distributed online nationwide in the USA. To date, no … See More

#recall #drugs #us

Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadalafil photo #1

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Arize male enhancement capsules - recalled due to undeclared Nortadalafil, USA

3 months ago •source www.fda.gov

Recall notice

"Today The World” is voluntarily recalling one lot of Arize Herbal Dietary Supplement capsules to the consumer level. FDA analysis has found the products to contain undeclared Nortadalafil. The product was distributed online via their website in the USA. To date, no adverse events have been reported. … See More

#recall #drugs #us

Arize male enhancement capsules - recalled due to undeclared Nortadalafil photo #1

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Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack of sterility assurance, USA

3 months ago •source www.fda.gov

Recall notice

Nurse Assist, LLC voluntary product recall (which included products supplied to Cardinal Health used in Covidien and Cardinal Health™ brand kits and trays), Cardinal Health issued a medical device recall on December 5, 2023, for its Covidien and Cardinal Health™ brand urology and operating room-specific kits and … See More

#medicaldevices #recall #us

Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack of sterility assurance photo #1

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TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence, USA

3 months ago •source www.fda.gov

Recall notice

Insight Pharmaceuticals is voluntarily recalling two lots of TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid to the consumer level due to elevated levels of benzene. The affected TING® 1% Tolnaftate Athlete’s Foot Spray Antifungal Spray Liquid lots were distributed nationwide in the United States through … See More

#recall #drugs #us

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Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine, USA

3 months ago •source www.fda.gov

Recall notice

Neptune Resources, LLC issues a voluntary recall of Neptune's Fix Elixir, Neptune's Fix Extra Strength Elixir, and Neptune's Fix Tablets Products Due to the Presence of Tianeptine. The products were distributed nationwide in the USA to wholesale and retail customers. Neptune Resources LLC's distribution channels have not … See More

#recall #drugs #us

Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tianeptine photo #1

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Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package, USA

3 months ago •source www.fda.gov

Recall notice

Azurity Pharmaceuticals, Inc. is voluntarily recalling one lot (F230169A) of Zenzedi® CII (dextroamphetamine sulfate tablets, USP) 30 mg to the consumer level. The product is being recalled due to a report from a pharmacist in Nebraska who opened a bottle of Zenzedi® 30 mg tablets and found … See More

#recall #drugs #us

Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package photo #1

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Robitussin Cough syrups - recalled due to microbial contamination, USA

3 months ago •source www.fda.gov

Recall notice

Haleon is voluntarily recalling eight lots of Robitussin Honey CF Max Day Adult and Robitussin Honey CF Max Nighttime Adult to the consumer level. The product is being recalled due to microbial contamination. To date, Haleon has not received any reports of adverse events related to this … See More

#recall #drugs #us

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Aligned Medical Solutions Convenience kits containing saline - recalled due to safety concerns, USA

3 months ago •source www.fda.gov

Recall notice

Aligned Medical Solutions, initiated a nationwide recall of Convenience kits containing saline because the Product cannot be verified as having the required sterility assurance level. Product(s) can be identified by the pack label inside the sterile barrier of the convenience kit. Aligned Medical Solutions distributed these kits … See More

#recall #medicaldevices #us