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East London Disco Centre, Romford Road, Aldersbrook, London, UK

Total all time reports:  1
Latest report: March 27, 2020 10:43 PM

Covid-19 possibly caused hospitalization

March 27, 2020 10:43 PM

“A tree surgeon I know through a friend is currently on a ventilator with symptoms probably caused by Covid-19. This a fit, 52-year-old guy who worked mostly outside in the City. See Less
Reported By SafelyHQ.com User

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SKAMANIA COUNTY COURTHOUS, 240 Nw Vancouver Ave, STEVENSON, WA, 98648, USA

May 9, 2021 12:00 PM

“Location of alleged hazard(s): Assessors office 240 Nw Vancouver Ave Stevenson, WA 98648-6447 Description of alleged hazard(s): Skamania County has chosen to make decisions regarding telecommuting opposite of the guidelines and recommendations of every agency that provides guidance to both local gov... See Moreernments and employers, including the Governor, Washington State Department of Health, WSAC, WCRP. Instead of minimizing health hazards by allowing telecommuting they are forcing people into small offices making a negligible work environment into a med/high risk environment. Neither Skamania County nor my department have provided or trained us on specific procedures for protection against COVID-19 infection as required per LNI. We have only received the LNI Basic Training PPT that says at the end our employer is required to provide specific procedures and our department will have additional guidelines to sign. On Monday, July 27th employees present in the Assessors were not wearing masks. office were wearing masks. One employee put one on after a while and the other one never put a mask on while I was in the office. Skamania County appears to only be considering the COVID-19 risks involved with having visitors in the building and not the risk of employees sharing an office.. They have put up screens on the counters but have not addressed the high risk of employee to employee infection.


Source: Osha.gov | Receipt Date: 2020-08-07
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Covid-19 OSHA Complaint, GENTLE DENTAL, 1710 Sw 9th Ave Ste 120, BATTLE GROUND, WA, 98604, USA

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May 9, 2021 12:00 PM

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Covid-19 OSHA Complaint, VANCOUVER SPECIALTY & REHABILI, 1015 N Garrison Rd, VANCOUVER, WA, 98664, USA

VANCOUVER SPECIALTY & REHABILI, 1015 N Garrison Rd, VANCOUVER, WA, 98664, USA

May 9, 2021 12:00 PM

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Source: Osha.gov | Receipt Date: 2021-02-17
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Covid-19 OSHA Complaint, LONG BEACH ELEMENTARY, 400 S Washington Ave, LONG BEACH, WA, 98631, USA

LONG BEACH ELEMENTARY, 400 S Washington Ave, LONG BEACH, WA, 98631, USA

May 9, 2021 12:00 PM

“1. Long Beach Elementary School does not have a properly functioning HVAC system, and staff is not permitted to open windows. 2. Long Beach Elementary have removed many of the crank handles on the windows to prevent anyone from opening them. Employees are concerned about the impact of this on emerge... See Morency procedures, as the building is in a tsunami zone. In the event of a near shore earthquake/tsunami, the emergency plan calls for all windows on the lower floor to be opened and all persons to go to the second floor. Opening the windows in this scenario is meant to stabilize the building as much as possible by allowing water to enter the building, equalizing pressure, instead of allowing water to build up pressure on the exterior of the building and potentially destabilizing it. Also, in the event of an armed intruder in the school, windows have proven to be a viable means of escape. This option is denied to us. Several classrooms nearly always have stagnant air. Employees have taped a thin string to the vents in several classrooms. They only move when someone walks by. Many classrooms get very warm during the day and are still warm the next morning. It doesn't seem like the system is functioning as it should. The school district has said the HVAC system is adequate, and will not provide any data to support this assertion. Another employee has requested an independent evaluation of the HVAC system, to which the district has said it is not needed. Employees would like an independent evaluation of the HVAC system, including air exchange rates. And would also like to be able to open windows to increase ventilation. LONG BEACH ELEMENTARY 400 S Washington Ave Long Beach, WA 98631


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Covid-19 OSHA Complaint, NUTRIEN AG SOLUTIONS INC, 1101 Midvale Rd, SUNNYSIDE, WA, 98944, USA

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May 9, 2021 12:00 PM

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May 9, 2021 12:00 PM

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Recent Interesting Reports

Pfizer BioNTech vaccine, Walgreens, Ohio 43, Streetsboro, OH, USA

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“Got the first dose of the Pfizer vaccine yesterday at Walgreens. Process was very smooth, no allergic reactions. Had some initial wooziness and lightheadedness 5 minutes after receiving the vaccine but may have just been anxiety.

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May 4, 2021 9:01 PM

“Company name: Hospira, Inc.
Brand name: Hospira, Inc.
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Reason of the recall: Due to visible particulate
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is voluntarily recallin... See Moreg lot DN9185 of Sterile Water for Injection, USP, 100 mL Single Dose Glass Fliptop Vial, to the hospital/institution level due to a confirmed customer report for a single vial with a visible particulate.

Hospira’s assessment of the potential risk to patients concluded that in rare instances the use of the impacted product can be associated with potential adverse events such as anaphylaxis, fever,    gastrointestinal disturbances, vein irritation, localized vein inflammation, phlebitis, end-organ granuloma, tissue ischemia, pulmonary emboli, and infarction.

To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for this lot. Sterile Water for Injection USP is a sterile, nonpyrogenic preparation of water for injection which contains no bacteriostat, antimicrobial agent or added buffer and is supplied only in single-dose containers. This parenteral preparation is indicated only for diluting or dissolving drugs for intravenous, intramuscular or subcutaneous injection, according to instructions of the manufacturer of the drug to be administered.

The NDC, Lot Number, Expiration Date, and Configuration details for Sterile Water for Injection, USP, is indicated in the table below and a photo of the product can be found at the end of this press release. The product lot was distributed nationwide to wholesalers/distributors/and hospitals in the United States from October to December 2020.

- Sterile Water for Injection, USP 100 mLbr Single-dose Glass Fliptop Vial. NDC: Vial: 0409-4887-25 | Carton: 0409-4887-99. Lot Number: DN9185. Expiration Date. 01 Apr 2023. Presentation: 100 mL, Single-dose Glass Fliptop Vial. Configuration: Tray of 25 vials.

Hospira, Inc., places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process. Hospira, Inc. has notified wholesalers/ distributors/hospitals by letter to arrange for return of any recalled product.

Wholesalers, distributors or hospitals with an existing inventory of the lot, which is being recalled, should stop use and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or hospital level/institution, please notify any accounts or additional locations which may have received the recalled product from you. Hospitals/Institutions should inform Healthcare Professionals in your organization of this recall. For additional assistance, call Stericycle at 1-800-805-3093 between the hours of 8 a.m. to 5 p.m. ET, Monday through Friday.

Healthcare Professionals with questions regarding this recall can contact Pfizer using the information in the link below.

Check the full recall details on fda.gov

Source: FDA
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April 12, 2021 1:00 PM

“Company name: J. M. Smucker Co.
Brand name: Meow Mix®
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FDA Recall date: April 12, 2021
Recall details: Orrville, OH – The J. M. Smucker Co. today announced a limited, voluntary recal... See Morel of two lots of Meow Mix® Original Choice Dry Cat Food (30LB bag) due to potential salmonella contamination. The Company has received no reports of pet illness or adverse reaction and has issued this recall out of an abundance of caution.

The impacted products were sold at select Walmart stores in IL, MO, NE, NM, OK, UT, WI, and WY. No other Meow Mix® products are impacted by this recall. If pet parents have products matching the following description in their possession, they should stop feeding it to their cats and dispose of it immediately. This information can be found on the bottom and back of each bag.

- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1081804. Best If Used By Date: 9/14/2022
- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1082804. Best If Used By Date: 9/15/2022

Check the full recall details on fda.gov

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April 21, 2021 6:01 PM

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SCAM, Alameda, CA, USA

Alameda, CA, USA

May 4, 2021 2:10 PM

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April 30, 2021 3:56 PM

“The same still saw scam as the other people on here. Same ad. It states $19.99 for that day and I ordered it. I also got the little manual wire saw. It said saw and accessories. It really hurts people on a fixed income. I hope they are proud of themselve See Less
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April 22, 2021 10:09 AM

“Yes. I also ordered the GTA 26 battery-powered electric chainsaw. I got the chain with handles. I was bantering back and forth with Chinese agent, who really does not know what to do except to try and get more money from me for an inferior chainsaw for $6. I ordered a GTA 26 chainsaw, Stihl brand. I... See Moregot the hand chainsaw (had never heard of using a chain by hand, but it is an actual thing). I don't think you can convert the hand chainsaw to using it with an actual chain saw anyway. The Chinese agent is trying appease me by saying I can get a chainsaw to use with the chain for $60. The website he sent me show a completely different chainsaw for 29.99 and he sent the actual picture of the See Less
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April 21, 2021 12:38 PM

“Blackcass.com is a total scam. My wife bought me what she thought was a mini electric chain saw. The site showed a sthil chain saw for $29.99 instead of $59.99. Not knowing the prices on tools she thought to surprise me. The next day I found her order in our computer and immediately contacted them a... See Morend tried to cancel it. They said it was too late as the order had already been processed. 10 weeks later we got a hand rose clipper instead. My wife had paid $37.99 for a clipper I got at Ace hardware before for $9.99 See Less
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April 30, 2021 6:01 PM

“Company name: Acella Pharmaceuticals, LLC
Brand name: Acella
Product recalled: NP Thyroid (Thyroid Tablets, USP)
Reason of the recall: Sub potency
FDA Recall date: April 30, 2021
Recall details: Acella Pharmaceuticals, LLC, is voluntarily recalling certain lots listed in the Tables 1 and 2 belo... See Morew of 15-mg, 30-mg, 60-mg, 90-mg and 120-mg NP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. The products are being recalled because routine testing has found these lots to be sub potent. The product contains less than 90% of the labeled amount of liothyronine (T3) and/or levothyroxine (T4).

Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent NP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight.

There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations, or cardiac arrhythmia.

To date, Acella has received 43 reports of serious adverse events that could possibly be related to this recall. NP Thyroid®, Thyroid Tablets, USP is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count and 7-count bottles. See product images below. To best identify the product, the NDC’s, Product Description, Lot Numbers, and Expiration Dates are listed on the link below.

These lots were distributed nationwide in the United States to Acella’s direct accounts, including wholesalers, pharmacies, and healthcare offices. Acella is proactively notifying its consignees to discontinue distribution of the above referenced lots being recalled and is arranging for return of all recalled products. Patients who are currently taking NP Thyroid® from the lots being recalled should not discontinue use without contacting their healthcare provider for further guidance and/or a replacement prescription.

Consumers with questions about the recall can email Acella Pharmaceuticals at recall@acellapharma.com or contact our representatives at 1-888-424-4341, Monday through Friday from 8:00 am – 5:00 pm ET. 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.

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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