Create a Report

Please provide report title
Please provide location
Please provide details

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
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!


IMPORTANT - 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.

Report by

Message us
WhatsApp

Recall

Updated:

Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol, USA

1 month ago •source fda.gov • details

Recall notice

Aruba Aloe Balm N.V. is voluntarily recalling 40 lots of Aruba Aloe Hand Sanitizer Gel Alcohol 80% and Aruba Aloe Alcoholada Gel to the consumer level. The products have been found to contain alcohol denatured with methanol. Products were distributed between 5/1/2021 and 10/27/2023 and sold in… See more

#recall #us

Aruba Aloe Hand Sanitizer Gel and Alcoholada Gel - recalled because they contain Methanol photo #1
322

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA

1 month ago •source fda.gov • details

Recall notice

Honeywell Safety Products USA, Inc. is voluntarily recalling Fendall 2000 Non-Sterile Eyewash Cartridge for the Fendall 2000 Eyewash Station. This recall is being conducted at the industrial consumer level. Honeywell’s supplier of the Fendall 2000 Non-Sterile Eyewash Cartridge has been found to be non-compliant with current good… See more

#recall #drugs #us

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance photo #1
322

ForeverMen Natural Energy Boost - recalled due to undeclared allergens, USA

1 month ago •source fda.gov • details

Recall notice

FAonline INC, is voluntarily recalling all lots within expiry of the ForeverMen capsules to the consumer level. FDA analysis founds these products to be tainted with sildenafil and Tadalafil. Sildenafil/Tadalafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of sildenafil in the… See more

#recall #allergicreaction #dietarysupplements #us #allergen

ForeverMen Natural Energy Boost - recalled due to undeclared allergens photo #1
322

ADM Animal Nutrition Chicken, Swine, Cattle, & Horse Feed - recalled due to elevated levels of minerals, USA

1 month ago •source fda.gov • details

Recall notice

ADM Animal Nutrition announced that specific lots may contain elevated levels of calcium, phosphorus, magnesium, sodium and/or chloride and may harm chickens, swine, beef cattle and equine. ADM (NYSE: ADM), is recalling the following products: Pen Pals® Chicken Starter-Grower 25-lb bag (Product No 70009ACF46); Pen Pals Chicken… See more

#recall #petfood #us

ADM Animal Nutrition Chicken, Swine, Cattle, & Horse Feed - recalled due to elevated levels of minerals photo #1

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence, USA

2 months ago •source fda.gov • details

Recall notice

Eugia US LLC (f/k/a AuroMedics Pharma LLC) has initiated a voluntary recall of lot number 3MC23011 of Methocarbamol Injection, USP 1000 mg/10 mL (100mg/mL) (Single Dose Vial) - 10mL Vial to the consumer level due to a customer product complaint for the presence of white particles floating… See more

#recall #drugs #us

AuroMedics Pharma Methocarbamol Injection - recalled due to Particulate Matter presence photo #1
323

Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk, USA

2 months ago •source fda.gov • details

Recall notice

Amneal Pharmaceuticals, LLC. Bridgewater, New Jersey (Amneal), is voluntarily recalling 4 lots (see table below) of Vancomycin Hydrochloride for Oral Solution, USP, 250 mg/5mL packaged in 80 mL, 150 mL, or 300 mL pack sizes, to the Consumer Level. Some bottles may have been overfilled which can… See more

#recall #drugs #us

Amneal Vancomycin Hydrochloride for Oral Solution - recalled due to super poteny risk photo #1
322

Equate and Nature's Bounty Folic Acid 1MG recalled due to exceeding intake limits, Canada

2 months ago •source recalls-rappels.canada.ca • details

Recall notice

Several brands of folic acid tablets have been recalled in Canada due to concerns that affected lots may exceed the acceptable intake limit for N-nitroso-folic acid. The recall involves multiple brands distributed across the country.

-Affected products
Brand: Compliments FOLIC ACID 1MG, Product Name: FOLIC ACID 1MG,… See more

#equate #drugs #recall #ca

Equate and Nature's Bounty Folic Acid 1MG recalled due to exceeding intake limits photo #1
86

GS Hamster/Gerbil pet food recalled due to Salmonella, Bushton, Kansas 67427, USA

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

Recall notice

Central Valley Ag Cooperative has voluntarily recalled its GS Hamster/Gerbil + Turmeric food due to a potential Salmonella contamination. The recall affects both animals and humans and is currently ongoing. The recalled product has been distributed in Kansas.

The recalled product is GS Hamster/Gerbil + Turmeric, sold… See more

#recall #bushton #kansas #us #salmonella

GS Hamster/Gerbil pet food recalled due to Salmonella photo #1

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter, USA

2 months ago •source fda.gov • details

Recall notice

Endo International plc announced today that one of its operating companies, Par Pharmaceutical, Inc. (Par), is voluntarily recalling one lot of Treprostinil Injection 20mg/20mL (1mg/mL) to the consumer level. The product is being recalled due to the potential for the presence of silicone particulates in the product… See more

#recall #drugs #us

Par Pharmaceutical Treprostinil Injection - recalled due to Silicone Particulate Matter photo #1
322

Megadyne Electrodes - Alert to Use for ages 12+ only, USA

2 months ago •source fda.gov • details

Recall notice

Megadyne issued a Class 1 Medical Device Correction to hospitals to limit the use of MEGA SOFT Universal and Universal Plus Reusable Patient Return Electrodes to patients aged 12 years or older after receiving reports of adult and pediatric patient burns following surgical procedures in which MEGA… See more

#recall #medicaldevices #us

Megadyne Electrodes - Alert to Use for ages 12+ only photo #1
322

Popular topics

#Lifted Boil Water Advisory #Power Outages #Boil Water Advisory #Drugs #Pet Food #Delivery #Starbucks #DreamBone Dog Treats #Online Scam #Unordered Package #Scam #First Energy #PG&E - Pacific Gas and Electric #Facebook Scam #Cedar Grove #Las Vegas
Last 30 days