Nestle Purina - Denver, CO, 4555 York St, Denver, CO 80216
Latest report:
18 individuals tested positive for Covid-19
3 years ago
18 individuals at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
8 Additional individuals at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
1 additional individual at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
3 Additional individuals at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
12 individuals tested positive for Covid-19
3 years ago
12 individuals at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
12 individuals tested positive for Covid-19
3 years ago
12 individuals at Nestle Purina Pet Care in Denver county tested positive for Covid-19. The outbreak began on 11/16/20
Source: colorado.gov
Source: colorado.gov
832
10 employees test positive for Covid-19
3 years ago
10 employees at Nestle Purina Petcare in Denver county tested positive for Covid-19. The outbreak began on 7/13/2020
Source: colorado.gov
Source: colorado.gov
832
Related Reports
Starbucks Metallic Mugs recalled due to burn and laceration hazards, USA
3 weeks ago •source www.nestleusa.com
Recall notice
Nestlé USA has announced a recall of 440,500 Starbucks-branded ceramic mugs due to safety concerns. The mugs, which have a metallic coating, pose a burn and laceration hazard if microwaved or filled with extremely hot liquid. The company has reported 12 incidents of the mugs overheating or
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breaking, resulting in 10 injuries. Nestlé USA is currently working closely with the U.S. Consumer Product Safety Commission on this recall.
The recalled mugs were sold in two sizes, 11 oz. and 16 oz., as part of four different gift sets during the 2023 holiday season. They were distributed at Target, Walmart, and Nexcom (military retail outlets) across the U.S. from November 2023 to January 2024. The recall does not affect any other Nestlé USA or Starbucks-branded products.
- Starbucks Holiday Gift Set with 2 Mugs (11 oz.). Retailer: Target.
- Starbucks Classic Hot Cocoa and Ceramic Mug (16 oz.). Retailers: Walmart, Nexcom.
- Starbucks Peppermint and Classic Hot Cocoa Ceramic Mug (16 oz.). Retailer: Target.
- Starbucks Holiday Blend Coffee and Mug (16 oz.). Retailers: Walmart, Nexcom.
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.
Source: www.nestleusa.com/media/pressreleases/metallicmugrecall
The recalled mugs were sold in two sizes, 11 oz. and 16 oz., as part of four different gift sets during the 2023 holiday season. They were distributed at Target, Walmart, and Nexcom (military retail outlets) across the U.S. from November 2023 to January 2024. The recall does not affect any other Nestlé USA or Starbucks-branded products.
- Starbucks Holiday Gift Set with 2 Mugs (11 oz.). Retailer: Target.
- Starbucks Classic Hot Cocoa and Ceramic Mug (16 oz.). Retailers: Walmart, Nexcom.
- Starbucks Peppermint and Classic Hot Cocoa Ceramic Mug (16 oz.). Retailer: Target.
- Starbucks Holiday Blend Coffee and Mug (16 oz.). Retailers: Walmart, Nexcom.
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.
Source: www.nestleusa.com/media/pressreleases/metallicmugrecall
304
W
user-wxcdd457
Anyone with any Sense, Knows that any metallic partial on Any container, will cause flames!! It’s not company’s fault. It’s the customers fault! Ignorance to the MAX!
- 3 weeks ago
- Reply
Covid cases in my area are high, Rolla, MO, USA
4 months ago •reported by user-cvttz511
Covid number are spiking in the area, especially in the FedEx and UPS terminal, Missouri S&T and Rolla public school's.
92
T
user-tnvv1773
costco optical lab employees are using and selling drugs in the lab
- 1 month ago
- Reply
Papa johns is not protecting their employees from COVID, Papa Johns Pizza, 9123 N Loop 1604 W, San Antonio, TX 78249, United States
8 months ago •reported by user-xwnh6111
Papa johns is not protecting their employees from COVID. I just got COVID and strep tested and it came back positive for both. They immediately told me to come back to work. This is completely unsanitary and unsafe for employees and customers. They are not following protocols
…
due COVID -19 and are disregarding everything just to have the correct amount of staffing.
218
Purina Pro Plan Veterinary Diets EL Elemental - recalled due to elevated Ingredient level, USA
1 year ago •source www.fda.gov
Recall notice
Nestlé Purina PetCare Company is expanding its voluntary recall of Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food due to a supplier error resulting in potentially elevated levels of vitamin D in two additional product lots, which precede the production dates of
…
the previously recalled lots. The original announcement was made on February 8, 2023. No other Purina pet care products are affected.
The expansion comes following an investigation prompted by Purina that uncovered new information about a production error from a U.S. supplier that was made only to this specific formula and resulted in potentially elevated levels of vitamin D. Vitamin D is an essential nutrient for dogs; however, ingestion of elevated levels can lead to health issues depending on the level of vitamin D and the length of exposure. Vitamin D toxicity may include vomiting, loss of appetite, increased thirst, increased urination, and excessive drooling to renal (kidney) dysfunction. A list of the additional impacted product is below. Bags of PPVD EL with the UPC Code and Production Code below should be immediately discarded.
Product: Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL)
UPC Code (*First 8 characters equal to): 38100 19190 – 8 lb / Production Code: 2213 1082 (NEW)
UPC Code (*First 8 characters equal to): 38100 19192 – 20 lb / Production Code: 2214 1082 (NEW)
The affected dry dog food was distributed throughout the United States by prescription only through veterinary clinics, Purina Vet Direct, Purina for Professionals, and other select retailers with the ability to validate a prescription.
Pet owners who purchased bags of the product listed above are asked to immediately stop feeding and throw it away in a container where no other animals, including wildlife, can get to it. If signs such as weight loss, excessive drooling, vomiting, loss of appetite or increased thirst or urination have occurred in their dog while eating this diet, pet owners should contact their veterinarian.
Veterinary and other retail partners should remove and destroy the affected product from their inventory.
In case your pet experiences harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Company name: Nestle Purina PetCare Company
Brand name: Purina
Product recalled: Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food
Reason of the recall: Potential Elevated Ingredient Level
FDA Recall date: March 10, 2023
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nestle-purina-petcare-company-expands-voluntary-recall-purina-pro-plan-veterinary-diets-el-elemental
The expansion comes following an investigation prompted by Purina that uncovered new information about a production error from a U.S. supplier that was made only to this specific formula and resulted in potentially elevated levels of vitamin D. Vitamin D is an essential nutrient for dogs; however, ingestion of elevated levels can lead to health issues depending on the level of vitamin D and the length of exposure. Vitamin D toxicity may include vomiting, loss of appetite, increased thirst, increased urination, and excessive drooling to renal (kidney) dysfunction. A list of the additional impacted product is below. Bags of PPVD EL with the UPC Code and Production Code below should be immediately discarded.
Product: Purina Pro Plan Veterinary Diets EL Elemental (PPVD EL)
UPC Code (*First 8 characters equal to): 38100 19190 – 8 lb / Production Code: 2213 1082 (NEW)
UPC Code (*First 8 characters equal to): 38100 19192 – 20 lb / Production Code: 2214 1082 (NEW)
The affected dry dog food was distributed throughout the United States by prescription only through veterinary clinics, Purina Vet Direct, Purina for Professionals, and other select retailers with the ability to validate a prescription.
Pet owners who purchased bags of the product listed above are asked to immediately stop feeding and throw it away in a container where no other animals, including wildlife, can get to it. If signs such as weight loss, excessive drooling, vomiting, loss of appetite or increased thirst or urination have occurred in their dog while eating this diet, pet owners should contact their veterinarian.
Veterinary and other retail partners should remove and destroy the affected product from their inventory.
In case your pet experiences harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Company name: Nestle Purina PetCare Company
Brand name: Purina
Product recalled: Pro Plan Veterinary Diets EL Elemental (PPVD EL) prescription dry dog food
Reason of the recall: Potential Elevated Ingredient Level
FDA Recall date: March 10, 2023
Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nestle-purina-petcare-company-expands-voluntary-recall-purina-pro-plan-veterinary-diets-el-elemental
303
Possible COVID-19 Symptoms, Cook Out, West Cumberland Street, Dunn, NC, USA
1 year ago •reported by user-rdqk1975
I started feeling symptoms yesterday morning after eating at this location in Dunn. The location was very dirty and none of the people wore masks. I have had to cancel my driver's test, dentist appointment, doctor's appointment and several other events.
| Symptoms: Other
13
Power Outage, Denver, Denver County, CO, USA
1 week ago
Xcel Energy shut off power to 55,000 Colorado customers across six counties Saturday for a controlled outage planned to last more than 24 hours, citing the dangerous wind conditions and wildfire risks this weekend. The outage map reported power outages affecting thousands of customers in their service
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area in Colorado on Saturday afternoon Apr 6. There are customers affected in Denver. Additionally, there are customers affected in Littleton, Longmont, Loveland, and Berthoud.
Outage link: www.outagemap-xcelenergy.com/outagemap/?state=CO#
Source: tx.my.xcelenergy.com/s/
Published: 2024-04-06
Outage link: www.outagemap-xcelenergy.com/outagemap/?state=CO#
Source: tx.my.xcelenergy.com/s/
Published: 2024-04-06
832
Order not received, Denver, Colorado, USA
2 months ago •reported by user-zjwc1282
I ordered from this company in good faith, I've never received anything. In checking with them they say its been shipped but the shipping number doesn't work. I've contacted them several times....no luck. Buyer beware!!!!
832
NEWINYEE INC, Denver, CO, USA
2 months ago •reported by user-pmxy2896
Never received order that was reported to have a transaction date 15 November 2022 at 02:16:59 UTC. The company sent the following tracking nunber (AT1463040****), l have tried this number for USPS, FEDX, and UPS. They all said it was not their tracking number. Newunyee says it
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was delivered on 2022-12-26, but we did not receive it. Trying to get the merchandise or our $44.94 amount back.
833
I received a package I didn't order, Denver, Colorado, USA
2 months ago •reported by user-krvyw545
I never ordered this package I don't even know where to come from or who would come from make some sense to me your speaker box tubes for the air hose and speaker boxes
832
Scam Alert, Denver, CO, USA
2 months ago •reported by user-jtfq2859
I placed an order on 19 December 2023 through Facebook and paid via my credit card. I have not heard anything since then.
832
Recent Interesting Reports
I didn't order this, Panama City, FL, USA
2 weeks ago •reported by user-wcyt2166
I didn't order this product want to send back I want my money back . I'm disabled and live on a fixed income and I would have never let any scam take from my account..it was over 200.00 I'm so upset I never want any of this again
76
An package from Heather s Motty, Union City, NJ, USA
3 weeks ago •reported by user-tjkd2133
I received a package from Heather s Motty Union City NJ today I have no idea what it is & no memory of ordering anything from them.
2.9K
Want a refund!, Deer Lodge, MT, USA
1 week ago •reported by user-hnvkg974
I received a package from Heathers Motty in Union City N.J. It was a PZGONE Streaming Device and the product is useless. I want a refund paid to my Paypal account.
1
Package I did not order, Tuscumbia, AL, USA
5 days ago •reported by user-tkcv3639
I received a black lace iefiel brand bra. The return address is Jerry(001)-yasfbara, 9208 Charles Smith Ave, rancho Cucamonga ca 91730.
43
Medline and Centurion Convenience kits - recalled due to lack of sterility, USA
1 week 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
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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/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-convenience-kits-containing-nurse-assist-09-sodium
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/safety/recalls-market-withdrawals-safety-alerts/medline-industries-lp-issues-nationwide-recall-convenience-kits-containing-nurse-assist-09-sodium
303
I got the wrong shoes, Rossz cipőt kaptam
1 day ago •reported by user-mdwq7578
I ordered EA7 shoes and received a scrap shoe for 24000 HUF if I do not get the price back I will file a complaint
I recieve this bottle, McComb, MS, USA
4 days ago •reported by user-mzjwb374
Came in a white package
15
SCAM - foveth. com, Oklahoma, USA
6 days ago •reported by user-dkbbz865
Got me with Judyblue jeans for $10 but I ordered and then saw reviews. Contacted them within the hour they say they may not be able to cancel, but I can return. I have already canceled my debit card, filed a contest for a fraudulent charge. So sick of dupe sites!!!
37
Honeywell Non-Sterile Eyewash Cartridge - recalled due to Non-compliance, USA
1 week 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
…
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/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
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/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
303
I am reporting a scam, Alabama, USA
2 weeks ago •reported by user-cxtv4755
I received something I did not order and was charged $198 on my debit card which I don't know how they got .
79
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