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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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VISTA GRANDE ELEMENTARY, 7001 CHAYOTE RD NE, RIO RANCHO, NM

Total all time reports:  3
Latest report: May 2, 2021 12:00 PM

2 employees tested positive for Covid-19

May 2, 2021 12:00 PM

“Multiple employees(2) at VISTA GRANDE ELEMENTARY in RIO RANCHO, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 05/02/2021,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

2 employees tested positive for Covid-19

April 15, 2021 12:00 PM

“Multiple employees(2) at VISTA GRANDE ELEMENTARY in RIO RANCHO, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 04/15/2021,

Source: env.nm.gov See Less
Reported By SafelyHQ.com User

2 employees tested positive for Covid-19

March 4, 2021 12:00 PM

“Multiple employees(2) at VISTA GRANDE ELEMENTARY, 7001 CHAYOTE RD NE in RIO RANCHO, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 03/04/2021,

Source: env.nm.gov 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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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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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


Source: Osha.gov | Receipt Date: 2021-02-18
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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

April 28, 2021 7:00 PM

“Company name: Scentsational Soaps & Candles, Inc.
Brand name: Ulta Beauty Collection & SS
Product recalled: Scented Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: April 28, 2021
Recall details: Scentsational Soaps & Candles, I... See Morenc., is voluntarily recalling 5 lots of Scentsational Soaps & Candles scented Hand Sanitizers from the Black and White Collection and Photo Real Collection and 3 lots of Ulta Beauty Collection scented Hand Sanitizer Spray packaged in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level. See products listed in the table below.

These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were distributed nationwide in the USA through Ulta Beauty, TJ Maxx, and Marshalls retail stores.

Risk Statement: 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 accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning. Exposure to benzene can occur through inhalation, oral, and skin.

There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. The affected bottles of hand sanitizer include a five-digit lot code printed on the bottle near the base or, in the case of the Ulta Beauty Collection product, a five-digit lot code followed by a single letter. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also attached to this notice.

Scentsational Soaps & Candles, Inc., has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in inventory. Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase.

Ulta Beauty has confirmed it has removed the recalled Ulta Beauty Collection product from its stores and online. Consumers with questions regarding this recall can contact our Customer Support Desk, 1-855-554-8050, M-F, during business hours 9:00 a.m. – 5:00 p.m. ET.

Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this 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. “As the owners of the company, my wife and I want to reassure consumers and our customers that we are doing absolutely everything possible to carry out this recall efficiently and effectively and ensure it does not happen again.” said Steve Morrison of Scentsational Soaps & Candles, Inc.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

April 22, 2021 10:09 AM

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May 4, 2021 9:01 PM

“Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: Sterile Water for Injection, USP, 100 mL Single Dose Glass Fliptop Vial
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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Reported By SafelyHQ.com User

April 29, 2021 5:31 PM

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April 19, 2021 9:01 PM

“Company name: Tenacore LLC
Brand name: Tenacore LLC
Product recalled: 2001 Tenacore Replacement CareFusion Alaris 8100 bezels
Reason of the recall: Potentially weakened elastic
FDA Recall date: April 19, 2021
Recall details: Company Announcement On February 24th, 2021, Tenacore LLC initiated a... See Morenationwide recall of 2001 Tenacore replacement CareFusion Alaris 8100 bezels due to potentially weakened plastic. A bezel with weakened plastic may, over time, lead to separation of the bezel post (recall issue) as well as other damage to the bezel (e.g., external cracking). The separation of one or more bezel posts may result in free flow, over infusion, under infusion or interruption of infusion. There is a related recall initiated by Becton Dickinson (BD). Information regarding that recall can be found using the following link: Becton Dickinson (BD) (CareFusion 303, Inc.) Recalls Alaris Pump Module Model 8100 Bezel Assembly Which Could Result in Free Flow, Over-Infusion, Under-Infusion, or Interruption of Infusion | FDA Consumers who have: Tenacore bezel parts (part number TIPA-8100-4410) with timestamp 5 and/or timestamp 6 should stop the distribution and use of these and return them to Tenacore LLC.
Alaris 8100 units that were serviced by Tenacore, or purchased from Tenacore between July 2020 and Feb 2020, should be inspected per the instructions described below to ensure that your device is not impacted. If it is, please return your device to Tenacore LLC.
Recalled bezels were manufactured from May 2020 to June 2020 and distributed from July 2020 through Feb 2021. The following products have been recalled:
Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

May 6, 2021 12:47 AM

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Reported By SafelyHQ.com User

April 12, 2021 1:00 PM

“Company name: J. M. Smucker Co.
Brand name: Meow Mix®
Product recalled: Meow Mix® Original Choice Dry Cat Food
Reason of the recall: Potential Salmonella Contamination
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

Source: FDA
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Reported By SafelyHQ.com User

Pfizer vaccine first dose, Fort Collins, CO, USA

Symptoms: Soreness
Fort Collins, CO, USA

April 13, 2021 11:07 PM

“I just received my first dose today. The shot was completely painless. I did not have any soreness in my arm until a few hours later. No side effects so far. I have been feeling good after the shot. My next one is in 21 days. See Less
Reported By SafelyHQ.com User

April 18, 2021 10:04 AM

“I have 2 sick, A week and a half ago Née bag of Kibbles and bits bistro and the Melody Just started about a week and a half ago now I have two dogs sick one with an IV in the hospital See Less
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Hospital

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Symptoms: Other Headache
Lauderhill, Florida, USA

April 25, 2021 12:35 PM

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