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Recent Interesting Reports
Tide, Gain, Ace, and Ariel Detergent Packets recalled due to Risk of Serious Injury, USA
2 weeks ago •source www.cpsc.gov
Recall notice
The recall involves Tide Pods, Gain Flings, Ace Pods, and Ariel Pods liquid laundry detergent packets packaged in flexible film bags. These products were manufactured between September 2023 and February 2024. The recall applies to bags containing 12 to 39 laundry detergent packets, with a variety of scents and types:
- Gain Flings Original
- Gain Flings Moonlight Breeze Scent
- Gain Flings Blissful Breeze Scent
- Gain Flings Spring Daydream Scent
- Gain Flings Plus Ultra Oxi
- Gain Flings Plus Odor Defense
- Tide Pods Original
- Tide Pods Spring Meadow Scent
- Tide Pods Light
- Tide Simply Pods Plus Oxi Boost
- Tide Pods Clean Breeze Scent
- Tide Pods Free & Gentle
- Tide Pods Oxi
- Tide Pods Ultra Oxi
- Ace Pods Clean Breeze
- Ace Pods Spring Meadow
- Ariel Pods Alpine Breeze
The products were sold At: Big Lots, CVS, Family Dollar, Home Depot, Sam’s Club, Target, Walmart, and other major stores nationwide and online at Amazon.com and other websites from September 2023 through present for between $5 (one 12 ct. bag) and $30 (four 39 ct. bags in a box). The total number of recalled units is approximately 8.2 million, with an additional 56,741 sold in Canada.
Please do not use this product if you have it at home and return it to the store where it was purchased for a full refund and a free replacement child-resistant bag to store the product.
If you or a loved one are harmed or experiencing any symptoms, it is important to report it. Reporting can help to detect & resolve outbreaks early and prevent others from being harmed, and enables better surveillance. If symptoms persist, seek medical care.
Source: www.cpsc.gov
I don’t have energy, Winding Lake Road, Sunrise, FL 33351, USA
3 days ago •reported by user-qjkn6782
I did not receive the order or receipt, Kfar Saba, Israel
1 week ago •reported by user-zjjg6114
toate reclemele care ajung pe facebook cu produse din china o sa le raportez
TECH 1 US, Flushing, Queens, NY, USA
3 weeks ago •reported by user-pcyvg797
Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
3 weeks ago •source www.fda.gov
Recall notice
The Fendall 2000 Non-Sterile Eyewash Cartridge is used for flushing or irrigating the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination. Product is contained in a 25-liter Ethylene-vinyl acetate (EVA) bag that is designed for use with the Fendall 2000 Eyewash Station. Only the Fendall 2000 refill cartridges are subject to this review, no other eyewash products. The saline eyewash solution contains purified water, benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate diabasic, and sodium phosphate monobasic. It is not marketed as sterile.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Region: USA. Quantity: 6,954.
- Fendall 2000 Non-Sterile Eyewash Cartridge. Manufacturer’s Product Number/ Catalog Number: 32-002050-0000. Manufacturing Dates: 11-Oct- 2021 through 21-Jun-2023. Expiration Date: 11-Oct-2023 through 21-Jun-2025. Canada. Quantity: 3,651
Honeywell Safety Products USA, Inc. is notifying its distributors and customers by email, telephone or certified mail and is requesting anyone with product in its inventory to destroy or dispose of all units subject to the recall. Customers / distributors / retailers that have Fendall 2000 Non-Sterile Eyewash Cartridges should stop selling, shipping, and using the product immediately and destroy or dispose of it. Customers with questions regarding this recall can contact Honeywell Safety Products USA, Inc. by telephone.
Risk Statement: Use of or exposure to the eyewash without seeking medical attention afterwards could result in a range of ocular infections such bacterial keratitis or endophthalmitis. Immunocompromised individuals, those sustaining ocular injuries that damage the corneal epithelium, and those sustaining penetrating ocular injuries are at higher risk of potential infection.
Company name: Honeywell Safety Products USA
Brand name: Fendall 2000
Product recalled: Non-Sterile Eyewash Cartridge
Reason of the recall: Non-compliance with current good manufacturing practice (cGMP) requirements.
FDA Recall date: April 05, 2024
Source: www.fda.gov
Keep sending product. Want to cancel., Wichita, KS, USA
1 week ago •reported by user-xytn2795
Facebook scam, Sepsiszentgyörgy, Romania
1 week ago •reported by user-pybv9827
It happened that on Facebook there was an advertisement for a solar camera one day that I had ordered and did not receive
I just received a bottle of Subgenix Bioribose that I didn’t order., Kings Mountain, NC, USA
3 weeks ago •reported by user-dvtj7516
Ring Scam, Yucca Avenue, Lancaster, CA, USA
3 weeks ago •reported by user-rzyzb777
Company on package says YOSHI DEALS