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Yuma, Arizona, United States
Updated: January 14, 2021 12:00 PM
Covid-19 OSHA Complaint, U.S. BORDER PATROL- YUMA SECTOR, 4035 SOUTH AVENUE A, YUMA, AZ, 85365, USA
U.S. BORDER PATROL- YUMA SECTOR, 4035 SOUTH AVENUE A, YUMA, AZ, 85365, USA
January 14, 2021 12:00 PM
“Employees who work in the sector buildings, sector offices, and personnel & finance command staff are reporting to work with CoVID-19 and/or symptoms of CoVID -19 and are not practicing social distancing, or wearing masks. There has been an increase in the number of employees who are testing positiv... See Moree for CoVID-19 because protections to prevent the spread are not being enforced.
Alleged Hazards: 1, Employees Exposed: 15
Source: Osha.gov | Receipt Date: 2020-07-09 See Less”
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Covid-19 OSHA Complaint, Yuma Regional Medical Center, 2400 S Avenue A, YUMA, AZ, 85364, USA
Yuma Regional Medical Center, 2400 S Avenue A, YUMA, AZ, 85364, USA
December 9, 2020 12:00 PM
“1. Employees who test positive for COVID-19 are asked to return to work, by the employer, within seven days because they no longer show symptoms. 2. Nurses at the Skilled Facilities are required to draw patient's blood, although patients who have tested positive are not isolated.
Alleged Hazards: 2... See More, Employees Exposed: 500
Source: Osha.gov | Receipt Date: 2020-07-08 See Less”
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Covid-19 OSHA Complaint, Sarah Farms, 2751 E Palo Verde St, YUMA, AZ, 85365, USA
Sarah Farms, 2751 E Palo Verde St, YUMA, AZ, 85365, USA
December 5, 2020 12:00 PM
“1 -The employer is not following current CDC and AZDHS guidelines to prevent the spread of COVID-19 in the workplace. 2 -Employees are not social distancing to prevent the spread of COVID in the workplace. 3 -Employees are exposed to extreme temperatures without water, rest and shade measures.
Alle... See Moreged Hazards: 3, Employees Exposed: 20
Source: Osha.gov | Receipt Date: 2020-09-23 See Less”
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8 individuals tested positive for Covid-19, Yuma High School, 400 S 6th Ave, Yuma, AZ 85364, USA
Yuma High School, 400 S 6th Ave, Yuma, AZ 85364, USA
October 1, 2020 12:00 PM
“8 individuals at Yuma High School in Yuma county tested positive for Covid-19. The outbreak began on 9/28/20
Source: colorado.gov See Less”
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Employee test positive for Covid-19, Crane Middle School, 4450 W 32nd St, Yuma, AZ 85364, USA
Crane Middle School, 4450 W 32nd St, Yuma, AZ 85364, USA
August 16, 2020 12:00 PM
“Crane School District confirmed Friday afternoon that a staff member at Crane Middle School had tested positive for COVID-19. The individual’s last workday was Aug. 4.
Source: yumasun.com See Less”
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Covid-19 OSHA Complaint, Buffalo Wild Wings, Yuma Palms Pkwy, Yuma, AZ 85365, USA
Buffalo Wild Wings, Yuma Palms Pkwy, Yuma, AZ 85365, USA
July 29, 2020 12:00 PM
“1. CDC guidelines have not been implemented and there are employees who have tested positive for the COVID-19. 2. Employees temperatures are checked at the start of each shift and if their temperatures are too high, employees are told to go cool off so that their temperature will record lower. 3. Em... See Moreployees who have tested positive are allowed to keep working. 4. Social distancing is not being enforced. 5. Masks are not required. 6. The cleaning and maintenance of the facility is not being enforced.
Source: Osha.gov | Receipt Date: 6/12/2020 See Less”
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Employee test positive for COVID-19, Yuma County Area Transit, 2715 E 14th St, Yuma, AZ 85365, USA
Yuma County Area Transit, 2715 E 14th St, Yuma, AZ 85365, USA
June 11, 2020 12:00 PM
“A Yuma County Area Transit (YCAT) employee has tested positive for COVID-19. The employee's last day of work was May 30
Source: kyma.com See Less”
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Employee tests positive for COVID-19, Dairy Queen Store, 2077 S 4th Ave, Yuma, AZ 85364, USA
Dairy Queen Store, 2077 S 4th Ave, Yuma, AZ 85364, USA
June 7, 2020 12:00 PM
“A Dairy Queen employee in Yuma has tested positive for COVID-19. If you visited the restaurant recently, please report it and any other location that you visited.
Source: kyma.com See Less”
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Pediatrics employee from YRMC tests positive for COVID -19, Yuma Regional Medical Center Pediatrics, 2359 S 22nd Dr, Yuma, AZ 85364, USA
Yuma Regional Medical Center Pediatrics, 2359 S 22nd Dr, Yuma, AZ 85364, USA
May 21, 2020 12:00 PM
“A Yuma Regional Medical Center Pediatrics Clinic worker at the 22nd Drive location has tested positive for COVID-19.
Source: kyma.com See Less”
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Workers in Arizona Prison have tested positive for Coronavirus, Yuma Territorial Prison Park, 220 Prison Hill Rd, Yuma, AZ 85364, United States
Yuma Territorial Prison Park, 220 Prison Hill Rd, Yuma, AZ 85364, United States
May 14, 2020 12:00 PM
“Trinity Services Group, a company that provides food services for jails and prisons in all 50 states, says four of its employees in Arizona have tested positive for COVID-19.
Source: kjzz.org See Less”
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Recent Interesting Reports
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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2 people found this review helpful
Sent wrong item and is a bad item!, Langlois, OR, USA
Langlois, OR, USA
January 16, 2021 3:36 PM
“I ordered a Stihl wood cutter and got an IWORKS mini chain saw that does not work. See Less”
Helpful
2 people found this review helpful
BLACKCASS.COM, Chainsaw not delivered, Ocala, FL, USA
Ocala, FL, USA
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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No product never came - Blackcass.com Chainsaw, Denver, Colorado, USA
Denver, Colorado, USA
January 4, 2021 7:46 PM
“I ordered a hand held chain saw on Dec 12th 2020. I was v
Charged $40.89 .
What did come in the mail
Was a extra chain, but no saw See Less”
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December 28, 2020 8:00 PM
“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 28, 2020
Recall details: Schaumburg, Illinois, Sunstar Americas, I... See Morenc. (SAI) is voluntarily recalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 12/31/2020 – 9/30/2022 to the consumer level. This product may be contaminated with the bacteria Burkholderia lata. This is an expansion of the recall initially announced on October 27, 2020. Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia.
To date, 29 adverse events have been reported to SAI related to this recall. Affected patients tested positive for Burkholderia lata infections, typically found in sputum cultures while under treatment for other serious medical conditions. Use of the contaminated product on patients with pre-existing respiratory conditions, including those infected with Covid-19, is particularly unsafe.
The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:
- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.
The product can be identified as shown in the images below Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.
Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers follow below:
-Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 16 fl.oz. Amber Bottles. NDC #: 052376-021-02. Product Code: 1789P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022
- Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Size/ Form: 4 fl.oz. Amber Bottles NDC #: 052376-021-04. Product Code: 1788P. Lots Recalled: ALL LOTS with expiration date from Dec. 31, 2020 through Sep. 30, 2022.
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. Sunstar is committed to delivering safe, fully compliant products of the highest quality and is taking necessary steps to prevent future occurrence of this issue. 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 See Less”
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Covid Super Spreader Gas Station, Chevron, New Macland Road, Powder Springs, GA, USA
Chevron, New Macland Road, Powder Springs, GA, USA
January 14, 2021 8:47 PM
“The owner refused to wipe down the countertop or the card swipe after me requesting him to do so after several people using it. I want everyone to refrain from going to this station since he does nothing to protect people during covid 19 See Less”
Helpful
1 person found this review helpful
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 See Less”
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January 12, 2021 2:00 PM
“Company name: Midwestern Pet Foods Inc.
Brand name: Sportmix, Nunn Better, ProPac, and Others
Product recalled: Dog and Cat Pet Food
Reason of the recall: Aflatoxin Levels Exceed Acceptable Levels
FDA Recall date: January 11, 2021
Recall details: Company Announcement Midwestern Pet Foods, Inc.,... See Moreof Evansville, IN is expanding its December 30, 2020 voluntary recall of certain dog and cat food products produced in our Chickasha Operations Facility to include all dog and cat pet food products made with corn products because those products may contain aflatoxin levels which exceed acceptable limits. Products were distributed nationally to online distributors and retail stores nationwide. Midwestern Pet Foods is expanding its voluntary recall out of an abundance of caution to help protect the health and safety of pets. The products recalled cover all that expire on or before July 9, 2022, depicted as “07/09/22” in the date code on the product, as discussed below. Products with expiration dates after 07/09/22 are not included in the recall. Aflatoxin is a toxin produced by the mold Aspergillus flavus, which can grow on corn and other grains used as ingredients in pet food. At high levels, aflatoxin can cause illness and death in pets. There have been reports of illnesses and deaths in dogs associated with certain lots of products. No human illnesses have been reported. Out of an abundance of caution, we have expanded this recall to cover all corn products containing pet foods with expiration dates prior to 07/09/22. If your pet shows signs of aflatoxin poisoning including sluggishness, loss of appetite, vomiting jaundice (yellowish tint to the eyes, gums, or skin due to liver damage), and/or diarrhea, contact a veterinarian immediately. Provide a full diet history to your veterinarian. It may be helpful to take a picture of the pet food label, including the lot number and best buy date. Lot code information may be found on the back of bag and will appear in a three‐line code, with the top line in format “EXP 03/03/22/05/L#/B###/HH:MM”.
As explained above, this recall covers ONLY product manufactured at Midwestern Pet Food’s Chickasha, Oklahoma facility. Note that the unique Chickasha Facility identifier is located in the date code as a“05” and “REG. OK‐PFO‐0005” at the end of the date code.
In addition, the only Midwestern Pet Foods facility that produces product bearing a three‐line date code is our Chickasha Facility (See first image below).
Retailers and distributors should immediately pull recalled lots from their inventory and shelves. Do not sell or donate the recalled products. Retailers are encouraged to contact consumers who have purchased the recalled products, if you have the means to do so (frequent buyer cards, etc.). Pet parents: do not feed the recalled products to your pets or any other animals. Destroy the food in a way that children, pets and wildlife cannot access them. Wash and sanitize pet food bowls, cups, and storage containers. Always ensure you wash and sanitize hands after handling recalled food or any utensils which have contacted recalled food. Contact Midwestern Pet Foods Consumer Affairs at 800‐474‐4163, ext. 455 from 7AM to 4PM Central Time, Monday through Friday, or by email at info@midwesternpetfoods.com for additional information. This voluntary recall is being conducted in cooperation with the U.S. Food and Drug Administration. All other Midwestern Pet Foods products are unaffected by this recall action. Recalled products are as follows, with lot codes found in Expanded Recall Lot Numbers:
Pro Pac Adult Mini Chunk
Pro Pac Performance Puppy
Splash Fat Cat 32%
Nunn Better Maintenance
Sportstrail 50
Sportmix Original Cat 15
Sportmix Original Cat 31
Sportmix Maintenance 44
Sportmix Maintenance 50
Sportmix High Protein 50
Sportmix Energy Plus 44
Sportmix Energy Plus 50
Sportmix Stamina 44
Sportmix Stamina 50
Sportmix Bite Size 40
Sportmix Bite Size 44
Sportmix High Energy 44
Sportmix High Energy 50
Sportmix Premium Puppy 16.5
Sportmix Premium Puppy 33
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
Scam on hand held Skil chain saw from Blackcass, Indianapolis, IN, USA
Indianapolis, IN, USA
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”
Helpful
1 person found this review helpful
January 1, 2021 9:01 PM
“Company name: Precision Dose Inc.
Brand name: GUM Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 15 mL unit dose cups
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: December 31, 2020
Recall details: Company Announcement Precision Dose,... See MoreInc. is voluntarily recalling all lots of Chlorhexidine Gluconate Oral Rinse USP, 0.12%, 15mL Unit Dose Cups bearing an expiration date from 1/31/2021 – 02/28/2022 (see specific lots below) to the consumer level. Precision Dose, Inc. was notified by the manufacturer of the product, Sunstar Americas, Inc., that this product may be contaminated with the bacteria Burkholderia lata.
From information provided by the manufacturer, Sunstar Americas, Inc., use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such pneumonia and bacteremia.
To date, no adverse events have been reported to Precision Dose, Inc. related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and the product impacted is:
- Distributed in cases each containing 3 shrink-wrapped plastic trays each with 10 unit dose cups, 30-pack. NDC 68094-028-62
- Distributed in cases each containing 10 shrink-wrapped plastic trays each with 10 unit dose cups, 100-pack. NDC 68094-028-61
Chlorhexidine Gluconate Oral Rinse was distributed nationwide in the USA to pharmaceutical wholesalers. Precision Dose, Inc. is notifying its consignees directly and is arranging for return of all recalled product. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.
Consumers with questions regarding this recall can contact Precision Dose, Inc. at 1 (800) 397-9228 (Monday-Friday, 8:00 AM to 4:30 PM Central Time) or by email to customercare@precisiondose.com. Consumers should contact their physician or healthcare provider if they have experienced problems that may be related to using this drug product. Affected products and lot numbers follow below: AFFECTED LOTS-Chlorhexidine Gluconate Oral Rinse USP, 0.12%
Check the full recall details on fda.gov
Source: FDA See Less”
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