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Second dose Pfizer Vaccine, Overland Park, KS, USA
April 26, 2021 7:12 PM
Overland Park, Kansas, United States
After second dose had terrible nausea and a migraine. Lasted full 12 hours then started subsiding. It came on very abruptly.
May 13, 2021 1:23 PM
“Received 1st dose of Pfizer vaccine on May 08 2021. Today is May 13. Symptoms the same as when I get a flu shot. Sore arm for 24 hours and felt tired the 2nd day. I have allergies to Sulpa drugs and anti-inflammatories - had to wait for 30 minutes on site after injections to see if I had a reactio... n. Nothing happened. :) ”
May 13, 2021 7:57 PM
“I am a woman in her 50's and I received the J&J vaccine on Monday 05.10.21 felt good right after arm a bit sore. The next day pretty fatigued low grade fever. ”
May 14, 2021 3:24 PM
“big welt in arm at injection site, sore for at least 5 days, immediately had enormous headache, took alieve for 2 days then it went away. Had bouts of hot and cold and was slow moving for at least a week. ”
March 28, 2021 6:25 PM
“Five hours after receiving her first Moderna vaccine, my 63 year old mother has chills, back ache, both legs ache, and fatigue. ”
Covid-19 OSHA Complaint, Make It Right Enterprises, Inc., 7584 W. 119th St, OVERLAND PARK, KS, 66213, USA
March 24, 2021 12:00 PM
“Employee working at the front counter was not wearing a mask when customers are dropping off cars for service.
Alleged Hazards: 1, Employees Exposed: 5
Source: Osha.gov | Receipt Date: 2021-03-09 ”
Covid-19 OSHA Complaint, Menorah Medical Center, 5721 W. 119th Street, OVERLAND PARK, KS, 66209, USA
February 3, 2021 12:00 PM
“1) Workers who are and or may be COVID19 positive are expected to continue working as long as they are asymptomatic. 2) The employer fails to notify employees of potential exposures to COVID19 positive patients or staff. Employees receive notification only when they begin to experience symptoms, the... y are then notified by the hospital of their contacts with COVID19 positive patients or staff. 3) The employer fails to provide COVID19 testing to asymptomatic employees or those employees experiencing limited symptoms when they have been in contact with COVID19 positive patients and/or co-workers. 4) Employees who are positive for COVID19 and are quarantined, are instructed to return to work without a confirmed negative COVID19 test. 5) Staff share a breakroom where they remove their masks, and they share desks, computers, phones, and bathrooms. Section 5(a)(1) of the OSH Act.
Alleged Hazards: 5, Employees Exposed: 11
Source: Osha.gov | Receipt Date: 2020-08-24 ”
January 21, 2021 12:00 PM
“Employees have tested positive for COVID-19, store does not sanitize properly after a positive test.
Source: Osha.gov | Receipt Date: 2020-12-28 ”
January 14, 2021 12:00 PM
“1. Employer does not have an established Respiratory protection program which is indicated by the issuing of N-95 respirators in absence of training, fit testing and medical evaluations. 1910.134
Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2020-10-19 ”
Covid-19 OSHA Complaint, Rehabilitation Hospital of Overland Park, 5100 Indian Creek Parkway, Overland Park, KS 66207, USA
November 25, 2020 12:00 PM
“1. Employer is not enforcing mask mandate requirements to prevent the spread of COVID-19 in the workplace. [General Duty 5(a)(1)] 2. Employer is not taking measures to provide appropriate personal protective equipment (PPE) to employees when interacting with known Persons Under Investigation (PUI) f... or COVID-19. [General Duty 5(a)(1)]
Source: Osha.gov | Receipt Date: 2020-09-28 ”
May 6, 2021 12:00 PM
“1. Employer is not enforcing mask wearing; workers kitchen area are not wearing masks properly. [General Duty 5(a)(1)]
Source: Osha.gov | Receipt Date: 2021-04-06 ”
Recent Interesting Reports
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 ”
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... g 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 ”
May 14, 2021 9:42 PM
“Amphitrite technology: I ordered a steel battery powered chainsaw as advertised on Facebook but instead I received a commando wire saw that works manually these people are scammers they got me for $27.85 the advertisement is misleading bastards. These people are crooks I wonder how many other four g... uys got scammed ”
May 10, 2021 1:47 PM
“I ordered two of the Outdoor orange saws off of fb on March I have not received either one. Invoice #489-10127461
Transaction # 1ym4274N33939154. I really need them as they were gifts. One of them was my husband's birthday present at the end of March They were ordered early and they removed t... he money from my account March 6, 2021. They still show them on FB. They also sent that email to me. After checking with others, information is not correct. Never delivered. ”
May 14, 2021 12:16 PM
“Ordered, paid for wood cutter chain saw. Scammed. Pissed!
Merchant Transaction ID# 77R972095R430100V ”
May 4, 2021 11:48 PM
“I was sent a comando chain instead this company is a fraud and PayPal let it happen 😡😡😡🤦🏽♀️🤬 ”
May 12, 2021 8:00 PM
“Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 12, 2021
Recall details: Company Announcement Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (... “Dibar”) is voluntarily recalling 27 lots of DIBAR Labs Hand Sanitizer packaged in 8oz (8-53090-00301-3 UPC) and 16 oz (8-53090-00302-0 UPC) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 1 and Label 1). Dibar is also voluntarily recalling 2 lots of ProtectoRx Hand Sanitizer packaged in 2oz (Lot Number LDHSN050720) and 16oz (Lot Number LDHSN050820) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 2 and Label 2). These products are being recalled after testing conducted by our firm revealed the presence of methanol.
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.
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 twelvedigit lot code printed on the bottle near the base.
The products can be identified by the label, scent, and lot code provided in the table at the end of this release. These products were distributed nationwide in the USA through S.E.N.D. LLC and its customers (Click in the link below Table 1). Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers (Click in the link below Table 2.). Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by a letter 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.
Consumers with questions regarding this recall can contact our Commercial Offices, +52 443-314-5369, M-F, during business hours 9:00 a.m. – 6:00 p.m. ET and/or email us to QA@dibarlabs.com. 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.
- 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
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. (Table 1. Lots distributed to S.E.N.D. LLC and its customers)
Check the full recall details on fda.gov
Source: FDA ”
May 13, 2021 8:18 AM
“I ordered the same chainsaw like many others.thru Facebook.
Battery-Powered Wood Cutter -
2021 Newst chainsaws-A perfect
tool for pruning shrubs and trees
Saw chain accessor
It supposedly shipped via USPS, however the what I presume number is bogus. ”
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 ”
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 ”