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Safety Reports: Drugs

Updated: September 11, 2023 11:57 AM

Staff and medical procedures are off way off, Lees Summit, MO, USA

9 months ago •reported by user-fhxtx618 • details

My gf came here due too a some one drugging her. Then the hospital does the same thing with anxiety medicine too force their claim that she need's too be admitted she was knocked out cold for 3 days some thing needs too be done also when… See more

#drugs #leessummit #missouri #us

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TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to Microbial Contamination, USA

9 months ago •source fda.gov • details

Recall notice

Church & Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Kids Strawberry Splash 16oz after the Company identified a microbial contamination due to the presence of yeast (Candida Parapsilosis) in lot #PA3083011 of the product, sold exclusively on Amazon between… See more

#recall #drugs #us

TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to microbial contamination photo #1

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WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

9 months ago •source fda.gov • details

Recall notice

Hua Da Trading Inc dba Wefun Inc. is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an ingredient known as a Phosphodiesterase Inhibitor (PDE-5) inhibitor found in FDA-approved products for the… See more

#drugs #recall #us

WEFUN Capsules - recalled due to Undeclared Sildenafil photo #1

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Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up, USA

9 months ago •source fda.gov • details

Recall notice

Marlex Pharmaceuticals, Inc. is voluntarily recalling one lot of Digoxin Tablets USP, 0.125mg and one lot of Digoxin Tablets USP, 0.25mg to the consumer level due to Label Mix-Up. Bottles of Digoxin Tablets, USP 0.125mg s are incorrectly labeled and contain Digoxin Tablets USP, 0.25mg Tablets. Bottles… See more

#recall #drugs #us

Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up photo #1

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Dr. Berne’s MSM drops and Mist - recalled due to Bacterial & Fungal Contamination, USA

10 months ago •source fda.gov • details

Recall notice

Dr. Berne’s Whole Health Products is voluntarily recalling all lots of MSM DROPS 5%,15% Solution, Dr. Berne’s Organic Castor Oil Eye Drops and Dr. Berne’s MSM MIST 15% Solution to the consumer level. FDA analysis has found one lot (lot 6786) of Dr. Berne's MSM DROPS 5%… See more

#recall #drugs #us

Dr. Berne’s MSM drops and Mist - recalled due to Bacterial & Fungal Contamination photo #1

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Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin), Wisconsin, United States

10 months ago •source fda.gov • details

Recall notice

Furst-McNess Company of Rockford, IL is recalling 18% Goat Starter feed due to an elevated level of Monovet® 90 (monensin). Monensin is an FDA-approved drug for use in certain animal feeds. However, if the feed contains excessive amounts of the drug, the feed can cause monensin toxicity… See more

#recall #drugs #us

Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin) photo #1

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Food Research International supplements - recalled due to E. Coli, California, USA

10 months ago •source accessdata.fda.gov • details

Recall notice

FDA announced the recall of 2975 bottles of Food Research International Uro Kid Support Capsules and Serious Brain Enhancer Capsules by Global Vitality Inc. due to potential E. Coli contamination. These products were distributed to a single consignee in California. Details about the consignee were not provided.… See more

#drugs #recall #california #us #e.coli

Food Research International supplements - recalled due to E. Coli photo #1

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Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results, USA

10 months ago •source fda.gov • details

Recall notice

Lupin Pharmaceuticals Inc. (Lupin) is voluntarily recalling two (2) lots of Tydemy (Drospirenone, Ethinyl Estradiol and Levomefolate Calcium Tablets 3mg/0.03mg/0.451 mg and Levomefolate Calcium Tablets 0.451 mg) to the patient (consumer/user) level due to out of specification (OOS) test results at the 12-month stability time point. Specifically,… See more

#recall #drugs #us

Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results photo #1

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Walgreens, Atlanta, GA, USA, Atlanta, GA, USA

11 months ago •reported by user-tjbbr958 • details

I’ve been taking a bad batch of vancomyosin, 125 mg. The capsules contain no powder. They contain a hard concrete like substance. They came from India. I got them there in Atlanta Georgia.

#drugs #walgreens #atlanta #georgia #us

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Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging, UK

11 months ago •source gov.uk • details

Recall notice

Tillomed Laboratories Limited is recalling one batch of Labetalol 200mg Tablets due to an error on the foil blister packaging. The incorrect aluminium foil blister packaging states Labetalol 100mg Tablets, however it should be labelled as Labetalol 200mg Tablets. This error has occurred at the primary packing… See more

#drugs #recall #gb

Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging photo #1

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Safety Reports: Drugs

Staff and medical procedures are off way off, Lees Summit, MO, USA

TheraBreath Kids Strawberry Splash Oral Rinse - recalled due to Microbial Contamination, USA

WEFUN Capsules - recalled due to Undeclared Sildenafil, USA

Marlex Pharmaceuticals Digoxin Tablets USP - recalled due to Label Mix-Up, USA

Dr. Berne’s MSM drops and Mist - recalled due to Bacterial & Fungal Contamination, USA

Furst-McNess Company 18% Goat Starter Medicated Feed - recalled due to Elevated level of Monovet 90 (monensin), Wisconsin, United States

Food Research International supplements - recalled due to E. Coli, California, USA

Lupin Tydemy oral contraceptive - recalled due to Out of Specification Results, USA

Walgreens, Atlanta, GA, USA, Atlanta, GA, USA

Labetalol 200mg Tablets - recalled due to an error on the foil blister packaging, UK

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