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Calamus, Iowa, United States

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Recent Interesting Reports

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Heather's Motty, 2207 Summit Avenue, Union City, NJ, USA

3 weeks ago •reported by user-gftfm286

I have received 2 different packages from Heather's Motty which I did NOT order. I will admit that I had looked at the product but because of my resent weight loss I wasn't sure of the size I should get so I never actually order this product, … See More
however have received 2 separate orders. What can I do to return and receive my money back?
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#unorderedpackage #delivery #2207summitavenue #unioncity #newjersey #us

Heather's Motty photo #1
2.8K
D

I got a ring today that I did not order, Lancaster, CA, USA is where it’s from

4 weeks ago •reported by user-djzyb457

So I went to the mailbox. It was in my mailbox a ring addressed to me that I did not order.
Sorry I just saw it was health issue. From Yoshi deals and I see a lot of other people got things they did not order.

#unorderedpackage #gramoissaniteringscam #delivery #lancaster #california #us

I got a ring today that I did not order photo #1
106
G

Subgenix Biorose powder I did not order, Fulfillment house, PO Box 5708 Tampa FL 33675

3 weeks ago •reported by user-gzfhx766

I did not order this product. It arrived with and unsealed at that.

On FB there was an ad for a free Burberry tote just have to pay shipping. Foolishly I clicked on it as soon as I clicked on it thinking the charge is going to … See More
be only for shipping 6.95$ or so they charge my card for $100 and try to do another separate charge for $60 or so I immediately called my bank and told them what happened. It was bait and switch. I also emailed this company and told him it was a bait and switch and they were fraud, and they kept on going back-and-forth with me that I want to keep part of. No I want all of my money back it’s fraud Then I received this powdery substance in the mail that I did not order or want. I said it was trying to off me.
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#scam #delivery #facebookscam

Subgenix Biorose powder I did not order photo #1

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

3 weeks ago •source www.fda.gov

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
manufacturing practice (cGMP) requirements. To date, Honeywell Safety Products USA, Inc. has not received any reports of adverse events related to this recall.

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
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#recall #drugs #us

Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance photo #1
303

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