Report by
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
Publix Super Market at Heather Island Plaza, 7578 SE Maricamp Rd, Ocala, FL 34472, USA
Total all time reports:
1
Latest report: July 26, 2020 12:00 PM
More incidents from:
Bakery
Grocery or supermarket
Coronavirus - Covid-19
Publix
7578, Southeast Maricamp Road
Ocala
Florida
United States
Employee test positive for Covid-19
July 26, 2020 12:00 PM
“A Publix employee at the 7578 SE Maricamp Rd. Ste. 100 location in Ocala has tested positive for COVID-19 Source: villages-news.com See Less”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
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”
Helpful
Recent Interesting Reports
Facebook Battery-Powered Wood Cutter x 1 SCAM, Chester, PA, USA
Chester, PA, USA
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”
Helpful
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”
Helpful
Pfizer Vaccine side effects, Lauderhill, Florida, USA
Symptoms: Other
Headache
Lauderhill, Florida, USA
April 25, 2021 12:35 PM
“I am having side effects. the left side of my mouth moves by it self, and air comes out. it did it back to back. my head and neck was hurting. also at times my beath stops for a brife second. these things never happened before. should i go to the hospital See Less”
Helpful
2 people found this review helpful
May 4, 2021 9:01 PM
“Company name: Hospira, Inc.
Brand name: Hospira, Inc.
Product recalled: 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and 1% Lidocaine HCl Injection, USP 30 mL
Reason of the recall: Due to mislabeling
FDA Recall date: May 04, 2021
Recall details: Hospira, Inc., a Pfizer company, is volun... See Moretarily recalling lot EG6023 of 0.5% Bupivacaine Hydrochloride Injection, USP 30 mL and lot EG8933 of 1% Lidocaine HCl Injection, USP 30 mL, to the hospital/institution level due to mislabeling whereby a portion of each lot was incorrectly labeled as the other product. This issue was identified as part of the investigation of a confirmed customer report.
Hospira’s assessment of the potential risk to patients concluded that the use of the impacted product is likely to cause adverse events of moderate to high severity. If 1% lidocaine is administered to the patient instead of 0.5% bupivacaine, the patient may be underdosed, leading to lack of efficacy with potential outcomes such as inadequate pain management, and failure of surgical anesthesia. If 0.5% bupivacaine is administered to the patient instead of 1% lidocaine, an overdose of bupivacaine may occur, which could lead to potential outcomes such as seizures; respiratory abnormalities including low oxygen and/or elevated carbon dioxide in the blood, too much acid in the body fluids, and temporary cessation of breathing; heart abnormalities such as heart contraction and/or relaxation issues, irregular heartbeat, slower than normal heart rate, abnormal heart rhythm in which the ventricles of the heart quiver instead of pumping normally, cardiac arrest and cardiac flatline.
To date, Hospira, Inc. has not received reports of any adverse events associated with this issue for these lots. 0.5% Bupivacaine Hydrochloride Injection, USP is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and obstetrical procedures. 1% Lidocaine HCl Injection, USP is indicated for the production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks when the accepted procedures for these techniques as described in standard textbooks are observed.
The NDC, Lot Number, Expiration Date, Strength and Configuration details for 0.5% Bupivacaine Hydrochloride Injection, USP and 1% Lidocaine HCl Injection, USP are in the table below and a photo of the products can be found at the end of this press release. The product lots were distributed nationwide to wholesalers, distributors, retailers, and hospitals in the United States, Puerto Rico and Guam from December 29, 2020 to April 15, 2021.
- 0.5% Bupivacaine Hydrochloride Injection, USP, Single Dose Teartop Vial. NDC: Vial: 0409-1162-19 Tray: 0409-1162-02. Lot number: EG6023. Expiration Date: 01 July 2022. Strength: 0.5%, 150 mg/30 mL (5 mg/mL). Configuration/ Count: Case Pack 2 x 25 Vials.
- 1% Lidocaine HCl Injection, USP Single Dose Teartop Vial. NDC: Vial: 0409-4279-16 Tray: 0409-4279-02. Lot number: EG8933. Expiration Date: 01 Aug 2022. Strength: 1%, 300 mg/30 mL (10 mg/mL). Configuration/ Count: Case Pack 2 x 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, retailers, and hospitals by mail to arrange for return of any recalled product.
Wholesalers, distributors or retailers with an existing inventory of the lot, which is being recalled, should stop administration and distribution and quarantine immediately. If you have further distributed the recalled product, to the wholesale or retail level, 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.
Check the full recall details on fda.gov
Source: FDA See Less”
Helpful
I received the moderna vaccine and strange side effects., Horseheads, New York, USA
Symptoms: Other
Skin Rash
Horseheads, New York, USA
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”
Helpful
SCAM, Alameda, CA, USA
Alameda, CA, USA
May 4, 2021 2:10 PM
“I bought a battery powered woodcutting saw from Kenyak. I recieved a chain with two rings. How can we stop these people. I bought this a couple months ago and today the ad is still running on USA today. Please help. Please stop these people. The add is still on USA today See Less”
Helpful
False advertising, Kingston, ON, Canada
Kingston, ON, Canada
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”
Helpful
1 person found this review helpful
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”
Helpful
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 See Less”
Helpful
2 people found this review helpful
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”
Helpful