1 individual tested positive for Covid-19, Poudre High School, 201 S Impala Dr, Fort Collins, CO 80521

2 years ago

1 individual tested positive for Covid-19, Poudre High School, 201 S Impala Dr, Fort Collins, CO 80521

201 South Impala Drive, Fort Collins, 80521 Colorado, United States

1 individual at Poudre High School in Larimer county tested positive for Covid-19. The outbreak began on 01-03-2021

Source: colorado.gov

#coronaviruscovid19 #201southimpaladrive #fortcollins #colorado #us

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I was staying at a shelter in Lockport Cares and there was a Christian pastor at the shelter. Guess again. I dialed an ubulanxe to go to the hospital because my teeth were bleeding.and I was coughing up blood. The woman told me I should not stay … See More
at Lockport Cares because I called an ambulance to go to the hospital.

I assume Lockport cares is possibly food poisoning people. Lockport cares gives you bag lunches , breakfast and dinner.

For 2 nights there is always corn or brownies during Bible study at 8pm at night.

I'm not allowed back because I claaid they were food poisoning people
I told the police when I dialed the ambulance.

My blood sugar was low and I was coughing up blood and my teeth were bleeding.

Warning. Lockport Cares does food poisoning


Also there is a hazard for COVID 19. The manager allows COVID 19 positive to stay there without mandatory mask
You are not required to wear mask indoors.amd of you are positive for covid 19, you are not required to wear a mask. There is a woman positive for covid 10 not wearing a mask everyday spreading her disease. Lockport Cares allows kids and married couples to stay the night also.

Lockport cares should be shut down for biohazard. Covid positive wear no masks. A mask is not required for covid positive people.

Warning.  | Symptoms: Cough
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Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th, … See More
2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.

There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. The reliability of positive test results is not affected.

Below is a list of the affected lots. The lot number can be found on the side of each test box along with the Use By date.
Lot Number: HB264, Use By Date: 1/1/2023, Number of Tests Shipped: 7,382
Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
Lot Number: HY264, Use By Date: 1/1/2023, Number of Tests Shipped: 1,920

There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.

Detect is notifying all customers and distributors affected by the recall. Anyone in possession of any unused tests from the affected lots should dispose of the tests. The outer packaging is recyclable while all the test components can be discarded as regular trash. Detect Hubs are not affected by the recall and do not need to be discarded.

Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.

Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.

Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots
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Power outages continue to affect Larimer County Customers. Fort Collins Utilities’s outage map is reporting about 1,868 customers affected by two power outages near Redwood Meadows and Hickory Village in Fort Collins on Friday morning Feb 23. The estimated time for restoration was listed at 2:00 a.m. … See More
MST. There is another outage affecting 501 customers in the Kensington area. The estimated time for restoration was approximately 9:15 p.m. Feb, 22 MST. Crews are working to restore power to the area.

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There were reports of a power outage in Larimer County, Colorado. Fort Collins Utilities’s outage map is reporting about 2,624 customers affected by scattered power outages in their service area on Thursday morning Feb 22. The Rigden Farm area in Fort Collins has 1,337 customers affected. The … See More
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Package I didn't order, Fort Collins, CO, USA

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Yes I received a package that I didn't order

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UNORDERD PACKAGE, Fort Collins, CO, USA

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I received SOME KIND OF PLASTIC HOLDER WITH SCRAF BUT I ordered 8 bed covers Did not receive them. Order came from AYLEN AMADOR, 1226 ANODOVER PARK EAST, TUKWILA WA 98188. Then I received another ONE A Horse Scraf that was also not my order I orderd … See More
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Recent Interesting Reports

Public Health Notice: An outbreak of Salmonella infections linked to geckos has been reported by the Public Health Agency of Canada. As of March 22, 2024 there are 35 confirmed cases of Salmonella Lome illness reported in this outbreak in the following provinces: British Columbia (2), Alberta … See More
(2), Saskatchewan (2), Manitoba (2), Ontario (18), Quebec (8) and New Brunswick (1).

Individuals became sick between March 2020 and January 2024. Five individuals have been hospitalized. No deaths have been reported. Individuals who became ill are between 0 and 84 years of age. Seven cases (20%) are in children 5 years of age or younger. More than half of the cases (66%) are female. The investigation is ongoing, as recent illnesses continue to be reported.

The outbreak, which has been ongoing since March 2020, has been traced back to two types of geckos: the crested gecko and the leopard gecko. Many of those affected reported either direct or indirect contact with these pets or their habitats prior to falling ill. Some individuals fell sick despite not handling the geckos themselves, but lived in the same house where the pets were kept. The same strain of Salmonella was found in a gecko habitat from the home of an ill individual.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

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I ordered it from Temu online, Singleton NSW, Australia

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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/safety/recalls-market-withdrawals-safety-alerts/honeywell-safety-products-usa-inc-issues-voluntary-worldwide-recall-honeywell-fendall-2000-non
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What is this for I didn't order it any information would be great.

Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. The recalled products were distributed in the following states: AL, AK, … See More
CA, CO, CT, DE, FL, GA, HI, ID, IL, IA, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NM, NC, NY, NJ, ND, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI, and WY through website. The recalled products were also sold via the below websites via courier direct delivery and mail order. Etsy, amazon, eva-nutrition, tejocotemexican, niwali, scienceofalpha. The recalling firm has not received any reported of illness.

Recalled Products include the following bearing below information. Product codes and expiration dates can be found on the bottom of the packaging.

Product Name: Eva Nutrition MexicanTejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Science of Alpha Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: NWL Nutra Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025
Product Name: Niwali Mexican Tejocote root, Serial No: 181121U, Mfg Date: 08/01/2023, Expiry Date: 06/2025

Per the safety alert update on 3/12/24, "The FDA continues to receive adverse event reports related to the products identified in this Safety Alert."

The recall was the result of a routine sampling program by the company which revealed that the finished products contained the yellow oleander. The company has ceased the production and distribution of the product as the company continues their investigation as to what caused the problem. Further the company is conducting comprehensive quality control and monitoring process.

Customers who have purchased these products should stop using them immediately and return them to the point of purchase for a full refund.

Ingestion of yellow oleander can cause neurologic, gastrointestinal, and cardiovascular adverse health effects that may be severe, or even fatal. Symptoms may include nausea, vomiting, dizziness, diarrhea, abdominal pain, cardiac changes, dysrhythmia, and more.

If you are experiencing symptoms after eating this product it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist seek medical attention.

Company name: Global Mix, Inc.
Brand name: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra
Product recalled: Tejocote Dietary Supplements
Reason of the recall: Product contains toxic yellow oleander.
FDA Recall date: April 10, 2024

Source: www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-tejocote-products-because-possible-health-risk
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