Create a Report

Please provide report title
Please provide location
Please provide details

Add more

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
Please provide email or phone

We do not show your email or contact info

Skip this step

Add photos or video

We recommend photos and videos to help explain your report

Add Photo/Video
Drop files here
Skip this step

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
Please provide email or phone

Thank you for your report!

The report was
successfully sent!

Edit my report

Your report is queued - it may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Safety Reports: Recall

Updated:

Real Time Reports

Recall notice

Alipotec King Alipotec Raiz de Tejocote - recalled due to Yellow oleander, USA

1 year ago •source fda.gov • details

Backstage Center is issuing a recall of approximately 280 Bottles of Alipotec Raiz de Tejocote, dietary supplements, that are labeled with the "Alipotec King" sticker. This recall is being initiated because FDA analysis found that the product contains toxic yellow oleander. The product has been exclusively distributed… See more

#amazon #dietarysupplements #recall #unitedstates

Recalls Alipotec King Alipotec Raiz de Tejocote - recalled due toYellow oleander Backstage Center is issuing... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls H&Natural Brand Products - recalled due to Yellow oleander San Luis, AZ, G.A. Mart dba H&Natural, is... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Nordic Naturals Baby’s Vitamin D3 - recalled due to Elevated level of Vitamin D3 dosage Nordic Natur... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

"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 #unitedstates

Recalls Sustain and Schwinnng male enhancement capsules - recalled due to undeclared Tadalafil and Nortadala... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

"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

#drugs #recall #unitedstates

Recalls Arize male enhancement capsules - recalled due to undeclared Nortadalafil "Today The World” is volun... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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

#recall #medicaldevices #unitedstates

Recalls Covidien and Cardinal Health Urology and room kits and trays Update - recalled due to potential lack... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls TING® 1% Tolnaftate Athlete’s Foot Spray recalled due to Benzene presence Insight Pharmaceuticals is... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Neptune’s Fix, Fix Elixir, Fix Extra Strength Elixir & Fix Tablets - recalled due to undeclared tian... photo #1
312   Comments Comment

Recall notice

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

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Zendedi dextroamphetamine sulfate tablets - recalled due to mislabeled package Azurity Pharmaceutica... photo #1
312   Comments Comment

Recall notice

Robitussin Cough syrups - recalled due to microbial contamination, USA

1 year ago •source fda.gov • details

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 #unitedstates

Recalls Robitussin Cough syrups - recalled due to microbial contamination Haleon is voluntarily recalling ei... photo #1
312   Comments Comment

Popular topics

#Unordered Package #Scam #Facebook Scam #Cedar Grove #Las Vegas #DreamBone Dog Treats #Pet Food #Online Scam #Delivery #Starbucks #Drugs