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Place of worship
Updated: January 22, 2021 7:52 AM
Moderna vaccine experience, First Baptist Church, Walton Way Extension, Augusta, GA, USA
Symptoms: Soreness
First Baptist Church, Walton Way Extension, Augusta, GA, USA
January 22, 2021 7:52 AM
“Organized, fast, friendly, helpful.
only side effect was a few hours of mild arm soreness. See Less”
Helpful
1 person found this review helpful
Covid-19 OSHA Complaint, The Greenhouse Christian Learning Center, 2959 Hermitage Road, WAYNESBORO, VA, 22980, USA
The Greenhouse Christian Learning Center, 2959 Hermitage Road, WAYNESBORO, VA, 22980, USA
January 21, 2021 12:00 PM
“Staff Members and visitors to the facility are not wearing face coverings.
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2020-11-30 See Less”
Helpful
Covid-19 OSHA Complaint, Rabbinical College of Telshe, 28400 Euclid Avenue, WICKLIFFE, OH, 44092, USA
Rabbinical College of Telshe, 28400 Euclid Avenue, WICKLIFFE, OH, 44092, USA
January 21, 2021 12:00 PM
“1. Students with COVID-19 are permitted to stay on campus. 2. There are rats and roaches in the dairy and meat kitchens. 3. The staff and students are not wearing masks.
Source: Osha.gov | Receipt Date: 2020-12-04 See Less”
Helpful
Covid-19 OSHA Complaint, Harvest Community Church, 17285 County Road 34, GOSHEN, IN, 46528, USA
Harvest Community Church, 17285 County Road 34, GOSHEN, IN, 46528, USA
January 21, 2021 12:00 PM
“COVID-19 response plan not in compliance with executive orders. COVID-19 response plan not being utilized and enforced. COVID-19 response plan being treated as optional. Refusal to update COVID-19 response plan as directed in executive order. Congregation regularly encouraged by church leadership to... See Moremeet in large groups in person, with or without masks and social distancing. Church staff trained to 'respect' the choices of individuals to mask up or not. Hospitality team shaking hands or otherwise physically touching as a greeting. Hospitality team not wearing PPE provided. Ropes separating seats in auditorium removed or ignored at whim to accommodate additional households less than 6 feet apart. Beverages served to people while standing and being consumed while walking and interacting without social distancing. Social gatherings before and after the religious services not curtailed.
Source: Osha.gov | Receipt Date: 2020-11-14 See Less”
Helpful
Covid-19 OSHA Complaint, The Greek Orthodox Metropolis of San Francisco, 1224 Alabama Street, VALLEJO, CA, 94590, USA
The Greek Orthodox Metropolis of San Francisco, 1224 Alabama Street, VALLEJO, CA, 94590, USA
January 21, 2021 12:00 PM
“The employer did not maintain an effective injury and illness prevention program in that the employer did not ensure that COVID-19 precautions per the state executive and local public health department orders are being followed at the workplace in the following instances: 1) The employer did not com... See Moreply with local county public health officer's orders prohibiting indoor gatherings. Ref T8 CCR §3205(c)(2)(F) 2) The employer did not ensure that all employees shall be separated from other persons by at least six feet to maintain physical distancing during church services or other gatherings. Ref 8CCR 3205(c)(6) 3) The employer did not provide face coverings and ensure they are worn by employees. Ref T8 CCR 3205(c)(7)(A) 4) The employer did not implement measures to communicate to non-employees the face coverings requirements on their premises during church services or other gatherings. Ref T8 CCR 3205(c)(7)(E)
Alleged Hazards: 4, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-12-23 See Less”
Helpful
17 individuals tested positive for Covid-19, Canyon View Vineyard Church, 736 24 1/2 Rd, Grand Junction, CO 81505
Canyon View Vineyard Church, 736 24 1/2 Rd, Grand Junction, CO 81505
January 21, 2021 12:00 PM
“17 individuals at Canyon View Vineyard Church in Mesa county tested positive for Covid-19. The outbreak began on 1/2/21
Source: colorado.gov See Less”
Helpful
5 individuals tested positive for Covid-19, Living Stone Christian Church, 2971 North Ave, Grand Junction, CO 81504
Living Stone Christian Church, 2971 North Ave, Grand Junction, CO 81504
January 21, 2021 12:00 PM
“5 individuals at Living Stone Christian Church in Mesa county tested positive for Covid-19. The outbreak began on 12/17/20
Source: colorado.gov See Less”
Helpful
16 individuals tested positive for Covid-19, The Downtown Vineyard Church, 402 Grand Ave, Grand Junction, CO 81501
The Downtown Vineyard Church, 402 Grand Ave, Grand Junction, CO 81501
January 21, 2021 12:00 PM
“16 individuals at Downtown Vineyard Church in Mesa county tested positive for Covid-19. The outbreak began on 12/26/20
Source: colorado.gov See Less”
Helpful
4 individuals tested positive for Covid-19, Sacred Heart of Jesus School, 1317 Mapleton Ave, Boulder, CO 80304
Sacred Heart of Jesus School, 1317 Mapleton Ave, Boulder, CO 80304
January 17, 2021 12:00 PM
“4 individuals at Sacred Heart of Jesus School in Boulder county tested positive for Covid-19. The outbreak began on 11/6/20
Source: colorado.gov See Less”
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6 individuals tested positive for Covid-19, St John's School, 700 S Franklin St, Denver, CO 80209
St John's School, 700 S Franklin St, Denver, CO 80209
January 17, 2021 12:00 PM
“6 individuals at St. John's Lutheran Church Preschool in Denver county tested positive for Covid-19. The outbreak began on 12/23/20
Source: colorado.gov See Less”
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Recent Interesting Reports
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”
Helpful
1 person found this review helpful
BlackCass battery operated chainsaw not received., Goodman, MO, USA
Goodman, MO, USA
January 8, 2021 12:49 PM
“On December 14, 2020 I ordered the Blackcass battery operated chainsaw. On January 8, 2021 I received a chain with two handles attached. See Less”
Helpful
December 29, 2020 1:59 PM
“I purchased the metre from boots chemist about 5 months ago and have just realised it measures in mmol/L I see there is a recall out on this metre, what should I do 💁♀️ 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”
Helpful
2 people found this review helpful
Scam, Blackcass.com chainsaw,, Nekoosa, WI 54457, USA
Nekoosa, WI 54457, USA
January 4, 2021 11:39 PM
“I ordered this saw on December 13th, on December 15th I recieved a confirmation notice the my purchase was on its way, today January 4th 2021 in the mail all I recieved was a chain. Is this a scam or what,and where is the rest of my purchased SAW????? See Less”
Helpful
1 person found this review helpful
December 30, 2020 9:21 AM
“The FDA is alerting pet owners and veterinary professionals about certain Sportmix pet food products manufactured by Midwestern Pet Foods, Inc. that may contain potentially fatal levels of aflatoxin. As of December 30, 2020, 28 deaths and 8 illnesses in dogs that ate the recalled product have been r... See Moreeported. This is an ongoing investigation. Case counts and the scope of this recall may expand as new information becomes available.
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. Pets experiencing aflatoxin poisoning may have symptoms such as sluggishness, loss of appetite, vomiting, jaundice (yellowish tint to the eyes or gums due to liver damage), and/or diarrhea. In severe cases, this toxicity can be fatal. In some cases, pets may suffer liver damage but not show any symptoms.
Pet owners should stop feeding their pets the recalled products listed below and consult their veterinarian, especially if the pet is showing signs of illness. The pet owner should remove the food and make sure no other animals have access to the recalled product. Sanitize pet food bowls, scoops, and storage containers using bleach, rinsing well afterwards with water, and drying thoroughly. There is no evidence to suggest that pet owners who handle products containing aflatoxin are at risk of aflatoxin poisoning.
Midwest Pet Food, Inc. already recalled the following lots of Sportmix pet food products:
- Sportmix Energy Plus, 50 lb. bag. Lots: Exp 03/02/22/05/L2 | Exp 03/02/22/05/L3 | Exp 03/03/22/05/L2
- Sportmix Energy Plus, 44 lb. bag. Lot: Exp 03/02/22/05/L3
- Sportmix Premium High Energy, 50 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Premium High Energy, 44 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 31 lb. bag. Lot: Exp 03/03/22/05/L3
- Sportmix Original Cat, 15 lb. bag. Lots: Exp 03/03/22/05/L2 | Exp 03/03/22/05/L3
Check the full outbreak announcement on fda.gov
Source: FDA See Less”
Helpful
2 people found this review helpful
Totally false advertising. Blackcass.com Chainsaw, Orlando, FL, USA
Orlando, FL, USA
January 4, 2021 10:32 PM
“Totally false advertising. I order two chainsaws and got two open 26" chains with straps on both ends. Not happy. This advertising was misleading and took over 30 days to receive this product in the mail. I am totally dissatisfied with this purchase and company. See Less”
Helpful
January 14, 2021 11:44 AM
“I wonder how many people were duped by this disreputable company! Guess I should know better than to order from a company I know nothing about! Shame on them for taking hard earned money during this day and time. And shame on Facebook for allowing them to advertise. See Less”
Helpful
1 person found this review helpful
Moderna COVID-19 Vaccine, no symptoms yet., Long Island City, Queens, NY, USA
Long Island City, Queens, NY, USA
January 14, 2021 8:51 PM
“I am a teacher and am authorized to get the Moderna vaccine. I made an appointment in Ridgewood 2 days ago. Appoint was at 5:20 but didn't get my shot until 7:40. The lines are extremely long at night. But the nurse said they are empty in the morning. Once you get inside it is very fast, everyone is... See Morevery helpful and you can sign up for your second vaccine. They make you wait 15 mins to make sure you're ok before you leave. I have no side effects from the shot and feel fine. See Less”
Helpful
3 people found this review helpful
Dreambones, chicken variety cause seizures, Pittsburgh, PA, USA
Pittsburgh, PA, USA
January 19, 2021 10:19 PM
“My puppy Angus, at age 5 months, ate a small amount of a dream bone on Jan 9, 2020 in the afternoon, and then started crying and pacing, not eating any more. About 5 pm, he refused to eat, and went to lie down in his bed, not begging at our table while we ate. He seemed stiff, and lay down with his... See Moreneck stretched out. Soon he was unresponsive and glassy-eyed, and stiff as a board. I took him to the Emergency vet, who did not think that there was any obstruction, and while at the vet's he improved, so I brought him home for observation. The vet said that it could be the onset of a neurological condition, or something in the Dreambone. He recovered, is now 18 months (it is more than a year later) and has never had a similar episode. By a process of elimination, it is probable that the Dreambone caused this reaction, and that it wasn't lethal because he only ate a small amount. See Less”
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3 people found this review helpful