Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Use camera
Select from library
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!
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)
Visit our learn pages for more helpful information or, email us: support@safelyhq.com
Goodbye! and best wishes in your recovery
Report by
Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

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)

If your report is poison related call 1-800-222-1222 for a free consultation with a live medical poisoning expert

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Slurping Turtle, East Liberty Street, Ann Arbor, MI, USA

Total all time reports:  2
Latest report: April 18, 2021 12:00 PM

An Employee test positive for Covid-19

April 18, 2021 12:00 PM

“An employee at Slurping Turtle located on East Liberty Street in Ann Arbor recently tested positive for Covid-19.

Source: twitter.com See Less
Reported By SafelyHQ.com User

An Employee test positive for Covid-19

April 6, 2021 12:00 PM

“An employee at Slurping Turtle located on East Liberty Street in Ann Arbor recently tested positive for Covid-19.

Source: twitter.com See Less
Reported By SafelyHQ.com User

Related Reports

Covid-19 OSHA Complaint, SKAMANIA COUNTY COURTHOUS, 240 Nw Vancouver Ave, STEVENSON, WA, 98648, USA

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
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, GENTLE DENTAL, 1710 Sw 9th Ave Ste 120, BATTLE GROUND, WA, 98604, USA

GENTLE DENTAL, 1710 Sw 9th Ave Ste 120, BATTLE GROUND, WA, 98604, USA

May 9, 2021 12:00 PM

“1- A patient was seen on Monday (08/24) for dental treatment. She was coughing heavily without a mask on during the procedure. Her husband called the next day and said she tested positive for covid. The manager told the dentist and the assistant that was in the room with her that they didn't need to... See Morequarantine. If they were wearing the personal protective equipment (PPE) they are fine. No office disinfection or sanitization was done. No patients or staff were notified. 2- We had a staff meeting this week. There was no social distancing. There were over 20 employees present. 3- The waiting room and the front counter are supposed to be wiped down and sanitized every hour. No one does it ever. It's not a safe office, way too many patients are seen at the same time. 4- We have a small lunch room. They don't limit the number of employees that are in there. One day there were 6 employees without masks eating lunch. There are no rules at this office. 5- There is no plexi glass at the front desk. We were told the company couldn't fund it. The employees that work at the front desk are within a couple feet of these patients.


Source: Osha.gov | Receipt Date: 2020-08-28
See Less
Reported By SafelyHQ.com User

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

“At Vancouver Specialty and Rehabilitative Care social distancing measures are not implemented in the kitchen area. There are too many employees in the kitchen and dish washing area at one time. Kitchen staff does not follow social distancing measures even when asked. Social distancing measures are n... See Moreot being taken seriously, some employees have been shaking hands, and placing hands on each other's shoulders. There is little to no cleaning in high volume kitchen areas, and also around exhaust, on walls, and under sinks. Along with the Covid-19 concerns, workplace violence is also a concern. Yelling is common in the workplace, often followed by empty threats. Bullying is also an issue. Managers or HR are not available until after 9am, and there is little to no supervision after meal service. The dry storage area is unsafe, with concerns that old plates could fall and injury an employee. VANCOUVER SPECIALTY & REHABILI 1015 N Garrison Rd Vancouver, WA 98664-1313


Source: Osha.gov | Receipt Date: 2021-02-17
See Less
Reported By SafelyHQ.com User

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


Source: Osha.gov | Receipt Date: 2021-02-18
See Less
Reported By SafelyHQ.com User

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

NUTRIEN AG SOLUTIONS INC, 1101 Midvale Rd, SUNNYSIDE, WA, 98944, USA

May 9, 2021 12:00 PM

“Lots of unguarded equipment both in the shop (in Toppenish} mixing plant, tank area and on the fertilizer trucks. There is no one on site that is first aid trained/CPR at Sunnyside or Toppenish. There is no safety committee at all. Only safety person is management and currently there is no one. WA C... See MoreOVID guide lines/required practices not being followed. Workers are unaware of safety. They do not know how or who to report injuries to. Lockout tagout program is only in English and the Hispanic employees don't understand it. There are no locks to use.


Source: Osha.gov | Receipt Date: 2021-03-09
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, CHIEF JOSEPH MIDDLE SCHOOL, 504 Wilson, RICHLAND, WA, 99352, USA

CHIEF JOSEPH MIDDLE SCHOOL, 504 Wilson, RICHLAND, WA, 99352, USA

May 9, 2021 12:00 PM

“Children in classrooms (specifically science) not being distanced by three feet.


Source: Osha.gov | Receipt Date: 2021-03-29 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, SHARIS OF NORTH YAKIMA, 1401 Lakeside Ct, YAKIMA, WA, 98902, USA

SHARIS OF NORTH YAKIMA, 1401 Lakeside Ct, YAKIMA, WA, 98902, USA

May 9, 2021 12:00 PM

“General Manager does not wear a mask inside of his office with the door closed and instructs me to come in with him and shut the door even if I try and stand outside. Assistant manager has pulled mask down to call out to kitchen workers, inches from my face. Workers wearing masks under their noses a... See Morend under their chins walk closely by me and talk with me in the kitchen and bakery area at the back of the restaurant. Cooks prepare food with masks below their chin and servers wear masks below the nose walking through the pass and through the bakery area. Off-duty employee walked from dining area to kitchen and bakery area and pulled down mask to socialize with staff.


Source: Osha.gov | Receipt Date: 2021-04-05
See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Tesoro, 770 N. Grand Ave, PULLMAN, WA, 99163, USA

Tesoro, 770 N. Grand Ave, PULLMAN, WA, 99163, USA

May 9, 2021 12:00 PM

“Business not requiring masks.


Source: Osha.gov | Receipt Date: 2020-06-30 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Eastern Washington University - Payroll Office, 526 5th Street, Cheney, WA 99004, USA

Eastern Washington University - Payroll Office, 526 5th Street, Cheney, WA 99004, USA

May 9, 2021 12:00 PM

“Management is directing low-level employees to enter a Covid-19 testing area without proper PPE and proper training. The only thing they are providing is a pair of gloves and disposable mask. Five facility employee's works in the area. They are not doing temperature check or screening.


Source:... See MoreOsha.gov | Receipt Date: 2021-03-09 See Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, INVESTMENTS BY DESIGN LLC, 3248 E Jump Off Rd Frnt, VALLEY, WA, 99181, USA

INVESTMENTS BY DESIGN LLC, 3248 E Jump Off Rd Frnt, VALLEY, WA, 99181, USA

May 9, 2021 12:00 PM

“Employer not wearing a mask or 6ft social distance rule after having covid.


Source: Osha.gov | Receipt Date: 2021-03-10 See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

2nd Dose Pfizer Vaccine, Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

Symptoms: Nausea Headache Dizziness Fatigue Body Ache Soreness
Parkland Hospital, Harry Hines Boulevard, Dallas, TX, USA

April 21, 2021 6:01 PM

“Day 1 after vaccination my symptoms were a headache, nausea, medicine head, dizzy spells and alittle fatigue. Day 2 after my second dose. My symptoms include the following, sore painful arm, nausea, slight headache, medicine head, body & muscle aches, lymph nodes appeared to be inflamed which caused... See Moremy ears to hurt. Felt like I had a mild case of the flu. Been miserable and missing 2 days of work because of this. See Less
Reported By SafelyHQ.com User

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
See Less
Reported By SafelyHQ.com User

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

Symptoms: Fatigue Lightheaded Muscle Pain Soreness
Walgreens, Ohio 43, Streetsboro, OH, USA

April 28, 2021 5:52 PM

“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.

Symptoms after 27 hours: sore arm, joint and muscle pain, fatigue.... See MoreFeeling warm/flushed but no fever. See Less
Reported By SafelyHQ.com User

April 29, 2021 10:25 AM

““I purchased this Stihl chain saw on Feb 4, 2021 from Blackcass but to date all I received was a chain with grips. I would like my saw as ordered or a full refund and they pay for shipping. See Less
Reported By SafelyHQ.com User

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
Reported By SafelyHQ.com User

Petmatrix Dreambone Dino Chews, Yulee, FL, USA

Symptoms: Vomiting Other
Yulee, FL, USA

April 27, 2021 9:13 AM

“We gave our dog the Dreambone Dino Chews on Sunday. On Tuesday we noticed he was wanting to go into his kennel and sleep. Tuesday evening he was acting odd with jerking movement, sticking his tongue out, oddly staring at the ceiling and refusing to drink water. We immediately took him to the vet whe... See Morere they induced vomiting, gave him antibiotics and an IV. He continued to not drink water in his own and show neurological behaviors that our vet said was focal seizures, lip-licking and star-gazing. The Dreambone treats were the only change in his diet. He would not drink water on his own for at least 3 days and he had focal seizures on and off for about 5 days. Do not give your dog any Petmatrix, Spectrum, or Dreambone product. They will poison your beloved pet. They package says they are made in China and when you google the company they are also made in Vietnam. See Less
Reported By SafelyHQ.com User
Doctor Visit: Yes
Diagnosis: Doctor visit

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
See Less
Reported By SafelyHQ.com User

May 6, 2021 12:47 AM

“This was all after waiting the 20 minutes before leaving within 5 minutes after getting in my car I felt a burning in my right foot that within 20 minutes was burning both feet and legs all the way. Burning in my body from the waste down for 4 hours then severe rash all over my body except my face. See Less
Reported By SafelyHQ.com User

April 29, 2021 5:31 PM

“I ordered a "Battery-Powered Wood Cutter x 1". The picture of my order was very similar to the one next to this report I am making. They sent me an email back telling my they had two options on the page and I chose to pay for some chain looking thing that looks like you can kill someone with it. And... See Morethey refuse to give me my money back. I have the order, email correspondence and photos of the product I ordered. They advertise in very large photos one thing and then have a very small photo in the corner of something else. You had no idea was even there. Until you don't get what you ordered, but in stead you get the tiny thing in the corner. I can supply all this to you if you can stop these thieves from continuing there false business practices. See Less
Reported By SafelyHQ.com User

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
See Less
Reported By SafelyHQ.com User