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Product: Evolve

Updated:

B

Fraud Alert, Ponte de Lima, Portugal

10 months ago •reported by user-bqng4272

I want to inform you that this site is a fraud I bought them and it took 35 days for them to send it and say that it was delivered, and no delivery was made, I complained and they sent it again, it took another 35 days … See More
and nothing, but they already told me that it was delivered, and I didn't receive it, I complained they said they could only return 60% of my payment and of course that's not what I will receive, and aunt don't buy from this seven, they are misleading thieves, I don't recommend it
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#scam #onlineshopping #delivery #onlinescam #pontedelima #vianadocastelodistrict #pt

1
J

Fraud Alert, Valongo, Portugal

1 year ago •reported by user-jfbd2878

I ordered a set of cast iron pans and paid 39.99€.
It was an opportunity, according to the announcement published on Facebook.
A month later, I received a Christmas ornament (a sock) that isn't even worth 1€!!!
I'm tired of complaining and the answers come from the … See More
email: info@vailivity.com. They asked me to return the item, which I did on 21/2/2023 and paid 5€ in postage.
Now they ask me for the shipping number but I didn't take a photo of the CTT stickers.
I ran out of money and without the pots!
They say that they will reimburse me the amount paid but, so far, nothing!!!!!!!!!!!!!!!
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#scam #delivery #facebookscam #valongo #portodistrict #pt

27
C

Fraud alert, 746 South Glasgow Avenue, Inglewood, CA, USA

1 year ago •reported by user-cdktf744

They pretended to be sellers in the Amazon and I bought a palette of electronic products with about 70 products and what I get is a charger cable and a hearing aid that the value here is $10.00 and I paid for the supposed box $37+send+taxi. What … See More
is their abuse. Think there are people who have less than you and the Christmas thief appears to steal what little of you to make wealth thief. Supposedly an offer for a frame box of electronic items of approximately 70 products, with a value of $37+sent + tax and what I receive is a charger cable and a headset that costs no more than $10.00 here. I want my money and an address to return this garbage.

I'm in Manati
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#unorderedpackage #scam #delivery #uspostalservice #southglasgowavenue #inglewood #california #us #evolve

alerta de fraude photo #1
2.8K

Sunshine Mills, Inc. Dog Food - recalled due to elevated levels of Aflatoxin, USA

2 years ago •source www.fda.gov

Recall notice

Company name: Sunshine Mills, Inc.
Brand name: Triumph, Evolve, Nature Farms, Elm and others
Product recalled: Dog Food
Reason of the recall: Elevated Levels of Aflatoxin
FDA Recall date: July 29, 2021
Recall details: Sunshine Mills, Inc. is issuing a voluntary recall of certain products due to … See More
potentially elevated levels of Aflatoxin above the acceptable limit. Aflatoxin is a naturally occurring by-product from the growth of Aspergillus flavus and can be harmful to pets if consumed in significant quantities. No illnesses have been reported in association with these products to date, and no other Sunshine Mills, Inc. pet food products are affected by this announcement. Products affected by this announcement:

- Triumph® Wild Spirit Craft Dog Food Deboned Chicken & Brown Rice Recipe (3.5 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Td2 11/Feb/2021. UPC Code: 073657 008736.
- Triumph® Wild Spirit Craft Dog Food Deboned Chicken & Brown Rice Recipe (30 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta2 11/Feb/2021. UPC Code: 073657 008750.
- Evolve® Classic Super Premium Food For Dogs Deboned Chicken & Brown (15 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta1 11/Feb/2021. UPC Code: 073657 380320.
- Wild Harvest® Premium Dog Food Chicken & Brown Rice Recipe (14 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta2 11/Feb/2021. UPC Code: 711535 509523.
- Nurture Farms® Natural Dog Food Deboned Chicken & Brown Rice Recipe (15 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta2 11/Feb/2021. UPC Code: 070155 113597.
- Evolve® Classic Super Premium Food For Dogs Deboned Chicken & Brown (30 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta2 11/Feb/2021. UPC Code: 073657 380313.
- Heart To Tail Pure Being® Natural Dog Food Deboned Chicken & Brown Rice Recipe (5 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Td2 11/Feb/2021. UPC Code: 4099100129441.
- Elm Pet Foods Naturals Chicken & Rice Recipe Dog Food (40 Lbs.). Lot Codes: Best If Used By 11 Feb 2022 Lot: Ta1 11/Feb/2021. UPC Code: 070155 225221.

The affected products were distributed in retail stores nationally. Retailers who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves. There are no other Triumph®, Evolve®, Wild Harvest®, Nurture Farms®, Pure Being®, or Elm products or other lot codes of these products affected by this recall.

While no adverse health effects related to these products have been reported, Sunshine Mills, Inc. has chosen to issue a voluntary recall of the above-referenced products as a precautionary measure in furtherance of its commitment to the safety and quality of its products. Pets that have consumed any of the above recalled products and exhibit symptoms of illness including sluggishness or lethargy combined with a reluctance to eat, vomiting, yellowish tint to the eyes or gums, or diarrhea should be seen by a veterinarian.

Consumers who have purchased the recalled products should discontinue use of the product and may return the unused portion to the place of purchase for a full refund.

Check the full recall details on www.fda.gov

Source: FDA
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#recall #dogfood #petfood #us #chicken #rice #brownrice #evolve

Sunshine Mills, Inc. Dog Food - recalled due to elevated levels of Aflatoxin photo #1
303

Infusion pumps and sets - recalled due to pumps may not deliver fluid at the accuracy specified in the instructions, USA

4 years ago •source www.fda.gov

Recall notice

Company name: CME America
Brand name: CMEAmerica BodyGuard
Product recalled: Infusion pumps and infusion sets
Reason of the recall: pumps may not deliver fluid at the accuracy specified in the instructions for use and infusion sets may under-deliver fluids
FDA Recall date: April 29, 2020
Recall details: … See More
CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), a leading global medical technology company, today issued the following update regarding two previously announced voluntary recalls, one related to all models of CMEAmerica BodyGuard® infusion pumps (FDA Recall Number: Z-1474-2020) and the other related to one of the device's infusion sets (FDA Recall Number: Z-1442-2020). Both previously announced recalls have now been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means the FDA believes that there is a reasonable probability that use of the recalled product(s) will cause serious adverse health consequences or death.

CME America previously notified customers affected by each recall and provided guidance on the potential impact to device performance when the affected products were used. Today, the company has issued an updated customer letter with additional guidance and to inform customers of the decision to suspend distribution of the BodyGuard® infusion pump system and to remove all existing products from the U.S. market.

The following is a summary of each individual product recall details:

CMEAmerica BodyGuard® Infusion Pump Recall

Details On Jan. 6, 2020, the company initiated a voluntary recall to notify customers of certain scenarios where pumps may not deliver fluid at the accuracy specified in the instructions for use that could result in a slower than expected delivery of medication (under-infusion), and/or faster than expected delivery of medication (over-infusion). Results indicate that pumps may have a delivery inaccuracy of up to ~13%. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America has assessed the potential risks associated with the issues outlined in the initial voluntary recall and determined that the BodyGuard® infusion pump may continue to be used in certain situations in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter until the pumps have been removed from the market.

To ensure customers retain access to critical medical equipment, particularly as the COVID-19 pandemic continues to evolve in the United States, CME America will implement a phased market removal and will continue to support the following activities in order to help limit clinical disruption and maintain patient focus during the COVID-19 pandemic: Use of products in the field in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter; Product service and repair activities at CME America and Authorized Service Depots; and Supply of infusion sets and accessories to support the infusion pumps remaining in the field.

The BodyGuard® infusion pump is designed to deliver fluids or medications into a patient's body in controlled amounts. The pump administers fluids through an infusion tubing set into a patient's vein or through other cleared routes of administration. The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital and home care environments. Typical applications for the BodyGuard® infusion pumps include but are not limited to chemotherapy, pain management, TPN, enteral nutrition fluids and antibiotics.

The recall and market removal affect approximately 28,400 devices, including all models of BodyGuard® infusion pumps listed below. These devices are primarily used in outpatient settings.
- BodyGuard 121
- BodyGuard 323
- BodyGuard 545*
- BodyGuard 575*
- BodyGuard 545 ColorVision
- BodyGuard 575 ColorVision
- CMExpress

*Note: These two pump models were inadvertently left out of the initial customer notification

CMEAmerica BodyGuard® Microset Infusion Set Recall

Details On Sept. 16, 2019, the company initiated a voluntary recall to notify customers that certain lots of BodyGuard® Microset infusion sets, when used with the BodyGuard® infusion pump, may under-deliver fluids up to 50% at the highest flow rates. At the time of the recall, CME America informed customers in the recall announcement to discard all remaining inventory of the infusion sets (Catalog #A120-003XYVA) and committed to reimbursing impacted customers. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America immediately stopped shipments of the affected infusion sets. This FDA classification does not change the previous guidance provided in the company's September recall announcement to customers. Affected products include:

CMEAmerica BodyGuard® Microset, Catalog #A120-003XYVA.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on www.fda.gov

Source: FDA
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#medicaldevices #us #evolve

Infusion pumps and sets - recalled due to pumps may not deliver fluid at the accuracy specified in the instructions photo #1
303

Recent Interesting Reports

Medline and Centurion Convenience kits - recalled due to lack of sterility, USA

3 weeks ago •source www.fda.gov

Recall notice

In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, for its Medline and Centurion branded convenience kits containing Nurse Assist 0.9% Sodium … See More
Chloride Irrigation USP and Sterile Water for Irrigation USP. The Nurse Assist recall was issued due to the potential for a lack of sterility, which could result in non-sterile products. Medline Industries, LP has received one adverse event associated with product manufactured by Nurse Assist.

Water-based medical products that are non-sterile and potentially contaminated could cause serious or life-threatening infections, including bloodstream, urinary tract, open wound/soft tissue, and respiratory infections. Patients who are elderly, critically ill, have weak immune systems (including newborn infants, pregnant women, and cancer patients), or have chronic diseases are particularly at risk of infection. However, other patients could also develop infections after exposure to contaminated water-based medical products.

The recall affects Medline and Centurion convenience kits that may be used at home by patients, caregivers, and home health providers, as well as convenience kits that may be used in medical settings for surgery or other medical procedures. Recalled kits include, but are not limited to, wound care kits, tracheostomy kits and catheter kits. A detailed list of recalled Medline and Centurion convenience kits, as well as an example of product labeling, can be found in the link below.

Consumers who have recalled product should stop using the product and contact Medline immediately.

Medline Industries, LP notified its direct distributors and consumers of the Nurse Assist recall by First Class Mail and email on 11/16/23, upon receipt of initial recall notification from Nurse Assist. Customers who received the recalled product were given instructions to quarantine all affected products immediately and provide Medline with a response regarding the affected quantity on hand. Upon confirmation of the affected quantity, Medline provided customers with over-labels to place on the affected inventory, with instructions for staff to remove the affected component before using the kit. The recall notification also instructed distributors and those who resold or transferred affected product to another company or individuals to notify their customers of this recall notification.

In case you experience harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Company name: Medline Industries, LP
Brand name: Medline and Centurion
Product recalled: Convenience kits
Reason of the recall: The potential for a lack of sterility
FDA Recall date: April 08, 2024

Source: www.fda.gov
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#recall #medicaldevices #us

Medline and Centurion Convenience kits - recalled due to lack of sterility photo #1
303
Y

Not the same as advertised, New Orleans, LA, USA

2 weeks ago •reported by user-ybpyc327

I order two of the nano tech bullet proof vest, when it arrived the material was a thin allistic material and not seeing hours this material could stop any for arm nor knife stabbing.. I want the correct item or my money back!! But it came from Heathers Morty’s out of Union City, New Jersey 07087

#scam #onlineshopping #onlinescam #delivery #neworleans #louisiana #us

Not the same as advertised photo #1
401

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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