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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Cortez, Colorado, United States

Updated: January 7, 2021 12:00 PM

January 7, 2021 12:00 PM

“3 individuals at Souder, Miller & Associates in Montezuma county tested positive for Covid-19. The outbreak began on 12/22/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

January 7, 2021 12:00 PM

“2 individuals at Hampton Inn Mesa Verde/Cortez in Montezuma county tested positive for Covid-19. The outbreak began on 1/4/21

Source: colorado.gov See Less
Reported By SafelyHQ.com User

January 7, 2021 12:00 PM

“2 individuals at Garcia & Co. Jewelers in Montezuma county tested positive for Covid-19. The outbreak began on 12/20/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

January 7, 2021 12:00 PM

“2 individuals at City Market #408 in Montezuma county tested positive for Covid-19. The outbreak began on 1/4/21

Source: colorado.gov See Less
Reported By SafelyHQ.com User

December 30, 2020 12:00 PM

“1 individual at Jiffy Lube in Montezuma county tested positive for Covid-19. The outbreak began on 11/15/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

December 7, 2020 12:00 PM

“3 individuals at Walmart #966 in Montezuma county tested positive for Covid-19. The outbreak began on 11/30/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

3 individuals tested positive for Covid-19, LivWell Enlightened Health Marijuana Dispensary, 1819 E Main St, Cortez, CO 81321

LivWell Enlightened Health Marijuana Dispensary, 1819 E Main St, Cortez, CO 81321

December 7, 2020 12:00 PM

“3 individuals at LivWell Enlightened Health in Montezuma county tested positive for Covid-19. The outbreak began on 11/12/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

December 7, 2020 12:00 PM

“6 individuals at Cortez Seventh-day Adventist Church in Montezuma county tested positive for Covid-19. The outbreak began on 11/7/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

November 27, 2020 12:00 PM

“3 individuals at Keesee Motor Co in Montezuma county tested positive for Covid-19. The outbreak began on 11/19/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

November 27, 2020 12:00 PM

“2 individuals at Jiffy Lube in Montezuma county tested positive for Covid-19. The outbreak began on 11/15/20

Source: colorado.gov See Less
Reported By SafelyHQ.com User

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London, UK

January 11, 2021 10:53 PM

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January 5, 2021 9:18 AM

“On 12/6/20, I had ordered 2 chainsaws as Christmas gifts for $65.97, but only received 2 vinyl pouches containing the chains to the saws. I contacted the seller to find out when I could expect the delivery on the saws, along with any tracking info they could provide on the items. A few days later th... See Moreey contacted me by email saying for me to check my order details, what I had ordered was the chains, and if I wanted the saws they were $89.99 each. So since I paid through PayPal, I will be reporting the issue and trying to retrieve my monies back. See Less
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January 4, 2021 3:23 PM

“I ordered a Stihl battery powered chainsaw as.shown on the advertisement on Facebook but instead I received a Commando Wire Saw that worked manually. I feel this needs to reported if not made right! The advertisement was very misleading. See Less
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January 8, 2021 6:01 PM

“Company name: Fresenius Kabi USA
Brand name: Fresenius Kabi
Product recalled: Ketorolac Tromethamine Injection, USP, 30 mg/mL
Reason of the recall: Presence of particulate matter
FDA Recall date: January 08, 2021
Recall details: Fresenius Kabi USA is voluntarily recalling a single lot of Ketoro... See Morelac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial to the user level due to the presence of particulate matter. Particulate matter was found in reserve sample vials. No adverse event reports have been received for the recalled lot, which was produced and sold in 2019.

Administration of products containing particulate matter could obstruct blood vessels and result in local irritation of blood vessels, swelling at the site of injection, a mass of tissue that could become inflamed and infected, blood clots traveling to the lung, scarring of the lung tissues, and allergic reactions that could lead to life-threatening consequences.

Ketorolac Tromethamine, a nonsteroidal anti-inflammatory drug, is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. The total combined duration of use of oral Ketorolac Tromethamine and Ketorolac Tromethamine Injection should not exceed 5 days. Listed below is a table of the recalled lot distributed nationwide in the United States to wholesalers, distributors, hospitals, and pharmacies between March 28, 2019 and September 3, 2019.

Product Name/Product size: Ketorolac Tromethamine Injection, USP, 30mg / mL, 1 mL fill in a 2 mL amber vial
NDC Number: 63323-162-01
Product Code: 160201
Batch Number: 6121083
Expiration Date: 02/2021
First Ship Date: 03/28/2019
Last Ship Date: 09/03/2019

Fresenius Kabi is notifying its distributors and customers by letter and asking customers and distributors to check their stock immediately and to quarantine and discontinue the use and distribution of any affected product. Distributors should notify their customers and direct them to quarantine and discontinue distributing or dispensing the affected lot, and to return the product to Fresenius Kabi.

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

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

December 27, 2020 3:02 PM

“False advertising misleading GTA 26 was ordered only received blades pictures of item was not item that I received See Less
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January 14, 2021 8:47 PM

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Reported By SafelyHQ.com User

January 5, 2021 5:07 PM

“I ordered a Skil handheld battery operated chainsaw and after several weeks received a pocket chainsaw in a small pouch. Never in any of the advertisements for the chainsaw that I ordered were there pictures of the pocket chainsaw I received. I even used PayPal to protect myself. This is clearly a... See Morescam and they need to be held accountable. This was Christmas present for someone and not only was it late, now it's not even what I ordered!! See Less
Reported By SafelyHQ.com User

January 4, 2021 7:46 PM

“I ordered a hand held chain saw on Dec 12th 2020. I was v
Charged $40.89 .
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Reported By SafelyHQ.com User

January 4, 2021 11:00 AM

“Company name: Essaar Inc.
Brand name: Soho Fresh
Product recalled: 70% Rubbing Alcohol
Reason of the recall: Contaminated with Methanol
FDA Recall date: January 04, 2021
Recall details: Company Announcement Essaar Inc. is voluntarily recalling lot 200528303 of Soho Fresh 70% Rubbing Alcohol... See Morein 33.81 oz. clear plastic bottles to the consumer level. FDA analysis of the product revealed it is contaminated with methanol. Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, Essar Inc. has not received any reports of adverse events related to this recall. The product is used as an external purpose use rubbing alcohol and is packaged in 33.81 oz. clear plastic bottles with lot number 200528303 and UPC 7502268987367.

Soho Fresh was distributed nationwide to retail stores. Essaar Inc. is notifying its distributors and customers by email and mail and is arranging for the return of all recalled product to Essaar Inc. Consumers that have product which is being recalled should stop using and discard or return to place of purchase or to Essaar Inc. contacting via email or phone or mailing address mentioned above for arrangements of return. Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund or call Essaar Inc. at 201-647-7606 Monday to Friday 9am to 5pm, Eastern Standard Time. Essaar Inc. can also be reached via email at essaarinc@yahoo.com.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax. Complete and submit the report Online.

Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. FDA’s update  

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

January 14, 2021 8:51 PM

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