Create a Report

Please provide report title

Please provide location

Make my report private

Please provide details

Alert regulators Alert business or product owner Get notifications for my case

Get alerts and updates for your case!

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

Please provide email or phone

Phone Number

Please provide email or phone

Show my report on homepage

We do not show your email or contact info

Skip this step

I agree to Terms & Conditions

Please accept our Terms & Conditions

Email or SMS copy of report

Enter below to get emailed a copy of your report, or sms a link to your report

Please provide email or phone

Phone number

Please provide email or phone

I agree to Terms & Conditions

Please accept our Terms & Conditions

Report by

Message us

Drugs

Updated: February 5, 2024 7:03 PM

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

2 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

303

Helpful
Follow
Add my report
Share
- Copy link

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

2 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

303

Helpful
Follow
Add my report
Share
- Copy link

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

TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence photo #1

303

Helpful
Follow
Add my report
Share
- Copy link

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

303

Helpful
Follow
Add my report
Share
- Copy link

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

303

Helpful
Follow
Add my report
Share
- Copy link

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

Robitussin Cough syrups - recalled due to microbial contamination photo #1

303

Helpful
Follow
Add my report
Share
- Copy link

Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns, USA

3 months ago •source www.fda.gov

Recall notice

Kilitch Healthcare India Limited is issuing an amendment in the last Nationwide press release dated November 13, 2023 issued for nationwide recall of various eye drops. These products were distributed nationwide in the USA to wholesalers, retailers, and via the product distributor, Velocity Pharma LLC.

There are … See More

#recall #drugs #us

Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns photo #1

303

Helpful
Follow
Add my report
Share
- Copy link

Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose, Canada

3 months ago •source recalls-rappels.canada.ca

Recall notice

Teva Canada Ltd. is recalling a single lot of its Pediatrix Acetaminophen Oral Solution for children due to an increased risk of overdose. The product was distributed nationwide in Canada. The product is available without a prescription and is used to relieve mild to moderate pain and … See More

#drugs #recall #ca

Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose photo #1

84

Helpful
Follow
Add my report
Share
- Copy link

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

3 months ago •source www.fda.gov

Recall notice

Leiters Health is voluntarily recalling 33 lots of products to the user level. The recalled batches of vancomycin IV bags, phenylephrine IV bags, and fentanyl IV bags are being recalled due to the potential for superpotency because they may contain twice the labeled amount of drug. The … See More

#recall #drugs #us

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency photo #1

304

Helpful
Follow
Add my report
Share
- Copy link

Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks, USA

4 months ago •source www.fda.gov

Outbreak

WARNING
On December 21, 2023, the FDA published a warning to consumers, healthcare providers, and pharmacists to not use counterfeit Ozempic (semaglutide) injection 1 milligram, which has entered the U.S. drug supply chain. This counterfeit product is labeled with lot number NAR0074 and serial number 430834149057. FDA … See More

#ozempic #drugs #us

Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks photo #1

305

Helpful
Follow
Add my report
Share
- Copy link

Create a Report

Get alerts and updates for your case!

Add photos or video

Email or SMS copy of report

Thank you for your report!

Report by

Drugs

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

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

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

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

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

Robitussin Cough syrups - recalled due to microbial contamination, USA

Lubricant Eye Drops & Multi-Symptom Eye Drops - recalled due to potential safety concerns, USA

Pediatrix Acetaminophen Oral Solution - recalled due to potential risk of overdose, Canada

Leiters Health Vancomycin, Phenylephrine & Fentanyl IV Bags - recalled due to potential double drug potency, USA

Semaglutide medications Marketed for Type 2 Diabetes or Weight Loss - Warning and risks, USA

I have a concern about this report:

Resolve my concern fast!

Thanks for your feedback!

Notify me when my concern is resolved

Thanks for your feedback!